Drug & Medication Database
Browse 18,617 FDA-approved medications with detailed information about uses, dosage, side effects, and interactions.
Penicillium Chrysogenum Var. Chrysogenum
penicillium chrysogenum var. chrysogenum
Dosage form: INJECTION, SOLUTION. Route: PERCUTANEOUS. Active ingredients: PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (.05 g/mL). Category: BLA.
Brands: Penicillium Notatum
Penicillium Digitatum
penicillium digitatum
Dosage form: SOLUTION. Route: INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS. Active ingredients: PENICILLIUM DIGITATUM (.0125 g/mL). Category: BLA.
Brands: Penicillium Digitatum
Penicillium Frequentans
penicillium frequentans
PURPOSE: For internal indications according to traditional homeopathic practice.
Brands: Symbio Quent Drops
Penicillium Notatum
penicillium notatum
PURPOSE: For internal indications according to traditional homeopathic practice.
Brands: Symbio Not Drops
Penicillium Roqueforti
penicillium roqueforti
PURPOSE: For internal indications according to traditional homeopathic practice.
Brands: Symbio Forti Drops
Penpulimab
penpulimab
11 DESCRIPTION Penpulimab-kcqx is a programmed death receptor-1 (PD 1)-blocking antibody. Penpulimab-kcqx is a humanized monoclonal IgG1 antibody with an approximate molecular weight of 150 kDa. Penpulimab-kcqx is produced in Chinese hamster ovary (CHO) cells. Penpulimab-kcqx injection is a sterile, preservative-free, clear to slightly opalescent, colorless to yellowish solution for intravenous infusion after dilution. Each vial contains 100 mg of penpulimab-kcqx in 10 mL solution.
Brands: Penpulimab Kcqx
Pentadecapeptide
pentadecapeptide
Dosage form: POWDER. Active ingredients: BPC-157 (1 kg/kg). Category: BULK INGREDIENT.
Pentadecapeptide Arginate
pentadecapeptide arginate
Dosage form: POWDER. Active ingredients: BPC-157 (1 g/g). Category: BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING.
Pentagastrin
pentagastrin
Manufactured by WYETH AYERST. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: PENTAGASTRIN (0.25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**). Application: NDA017048.
Pentamidine Isethionate
pentamidine isethionate
DESCRIPTION Pentamidine isethionate for injection, an anti-protozoal agent, is a sterile, nonpyrogenic, lyophilized product. After reconstitution, it should be administered by intramuscular (IM) or intravenous (IV) routes (see DOSAGE AND ADMINISTRATION ). Pentamidine isethionate is a white crystalline powder soluble in water and glycerin, slightly soluble in alcohol and insoluble in ether, acetone, and chloroform.
Brands: Pentamidine Isethionate
Pentazocine
pentazocine
Dosage form: POWDER. Active ingredients: PENTAZOCINE (1 kg/kg). Category: BULK INGREDIENT.
Pentazocine And Naloxone
pentazocine and naloxone
DESCRIPTION Pentazocine and Naloxone Hydrochloride Tablets, USP contain pentazocine hydrochloride, USP, a partial opioid agonist, equivalent to 50 mg base and is a member of the benzazocine series (also known as the benzomorphan series), and naloxone hydrochloride, USP, an opioid antagonist equivalent to 0.5 mg base. Pentazocine and Naloxone Hydrochloride Tablets, USP are an analgesic for oral administration.
Brands: Pentazocine And Naloxone
Pentazocine Hydrochloride
pentazocine hydrochloride
Dosage form: POWDER. Active ingredients: PENTAZOCINE HYDROCHLORIDE (1 kg/kg). Category: BULK INGREDIENT.
Pentazocine Hydrochloride And Naloxone Hydrochloride
pentazocine hydrochloride and naloxone hydrochloride
DESCRIPTION Pentazocine and Naloxone Tablets, USP contain pentazocine hydrochloride, USP, a partial opioid agonist, equivalent to 50 mg base and is a member of the benzazocine series (also known as the benzomorphan series), and naloxone hydrochloride, USP, an opioid antagonist equivalent to 0.5 mg base. Pentazocine and Naloxone Tablets, USP are an analgesic for oral administration.
Brands: Pentazocine And Naloxone
Pentazocine Lactate
pentazocine lactate
Manufactured by HOSPIRA. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: PENTAZOCINE LACTATE (EQ 30MG BASE/ML). Application: NDA016194.
Pentetate Calcium Trisodium
pentetate calcium trisodium
11 DESCRIPTION Pentetate calcium trisodium injection contains the sodium salt of calcium diethylenetriaminepentaacetate. Pentetate calcium trisodium is also known as trisodium calcium diethylenetriaminepentaacetate and is commonly referred to as Ca-DTPA. It has a molecular formula of Na 3 CaC 14 H 18 N 3 O 10 and a molecular weight of 497.4 Daltons.
Brands: Pentetate Calcium Trisodium
Pentetate Calcium Trisodium Yb-169
pentetate calcium trisodium yb-169
Manufactured by 3M. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: PENTETATE CALCIUM TRISODIUM YB-169 (2mCi/ML). Application: NDA017518.
Pentetate Zinc Trisodium
pentetate zinc trisodium
11 DESCRIPTION Pentetate zinc trisodium injection contains the sodium salt of zinc diethylenetriaminepentaacetate. Pentetate zinc trisodium is also known as trisodium zinc diethylenetriaminepentaacetate and is commonly referred to as Zn-DTPA. It has a molecular formula of Na 3 ZnC 14 H 18 N 3 O 10 and a molecular weight of 522.7 Daltons.
Brands: Pentetate Zinc Trisodium
Pentetic Acid
pentetic acid
Dosage form: POWDER. Active ingredients: PENTETIC ACID (1 kg/kg). Category: BULK INGREDIENT.
Pentetrazole
pentetrazole
Dosage form: POWDER. Active ingredients: PENTETRAZOL (1 kg/kg). Category: BULK INGREDIENT.
Pentetreotide
pentetreotide
Dosage form: POWDER. Active ingredients: PENTETREOTIDE (25 kg/25kg). Category: BULK INGREDIENT.
Pentobarbital
pentobarbital
Manufactured by SCIEGEN PHARMS. Dosage form: ELIXIR. Route: ORAL. Active ingredients: PENTOBARBITAL (18.2MG/5ML). Application: ANDA083244.
Pentobarbital Sodium
pentobarbital sodium
DESCRIPTION The barbiturates are nonselective central nervous system depressants which are primarily used as sedative hypnotics and also anticonvulsants in subhypnotic doses. The barbiturates and their sodium salts are subject to control under the Federal Controlled Substances Act (See " Drug Abuse and Dependence " section). The sodium salts of amobarbital, pentobarbital, phenobarbital, and secobarbital are available as sterile parenteral solutions.
Brands: Pentobarbital Sodium
Pentolinium Tartrate
pentolinium tartrate
Manufactured by WYETH AYERST. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: PENTOLINIUM TARTRATE (10MG/ML). Application: NDA009372.
Pentosan Polysulfate Sodim
pentosan polysulfate sodim
Dosage form: POWDER. Active ingredients: PENTOSAN POLYSULFATE SODIUM (1 kg/kg). Category: BULK INGREDIENT.
Pentosan Polysulfate Sodium
pentosan polysulfate sodium
DESCRIPTION Pentosan polysulfate sodium is a semi-synthetically produced heparin-like macromolecular carbohydrate derivative, which chemically and structurally resembles glycosaminoglycans. It is a white odorless powder, slightly hygroscopic and soluble in water to 50% at pH 6.
Brands: Elmiron
Pentosan Polysulfte Sodium
pentosan polysulfte sodium
Dosage form: POWDER. Active ingredients: PENTOSAN POLYSULFATE SODIUM (1 kg/kg). Category: BULK INGREDIENT.
Pentostatin
pentostatin
DESCRIPTION NIPENT ™ (pentostatin for injection) is supplied as a sterile, apyrogenic, lyophilized powder in single-dose vials for intravenous administration. Each vial contains 10 mg of pentostatin and 50 mg of Mannitol, USP. The pH of the final product is maintained between 7.0 and 8.5 by addition of sodium hydroxide or hydrochloric acid.
Brands: Nipent
Pentoxifylline
pentoxifylline
DESCRIPTION Pentoxifylline Extended-Release Tablets USP for oral administration contain 400 mg of the active drug and the following inactive ingredients: hypromellose, povidone, talc, magnesium stearate, maltodextrin, polyethylene glycol, titanium dioxide, triacetin, D&C yellow #10 aluminum lake and FD&C yellow #6 in an extended-release formulation.
Brands: Pentoxifylline
Pentoxifyllline
pentoxifyllline
Dosage form: POWDER. Active ingredients: PENTOXIFYLLINE (1 kg/kg). Category: BULK INGREDIENT.
Medical Disclaimer
This drug database is for informational purposes only. Drug information is sourced from the FDA National Drug Code Directory and Structured Product Labeling. Always consult with a healthcare provider before starting, stopping, or changing any medication.