Ceruletide Diethylamine
Generic Name: ceruletide diethylamine
Manufactured by PHARMACIA AND UPJOHN. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: CERULETIDE DIETHYLAMINE (0.02MG/ML). Application: NDA018296.
Overview
Manufactured by PHARMACIA AND UPJOHN. Dosage form: INJECTABLE. Route: INJECTION. Active ingredients: CERULETIDE DIETHYLAMINE (0.02MG/ML). Application: NDA018296.
Dosage
Available as injectable for injection use.
Related Medications
Arnica Montana, Aurum Metallicum, Cactus Grandiflorus, Calcarea Carbonica, Lachesis Mutus, Natrum Muriaticum, Nux Vomica, Phosphorus, Solidago Virgaurea,
arnica montana, aurum metallicum, cactus grandiflorus, calcarea carbonica, lachesis mutus, natrum muriaticum, nux vomica, phosphorus, solidago virgaurea,
Standardized Chemical Allergen [EPC]
INDICATIONS: May temporarily relieve symptoms due to fluid retention and anxiety.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Fibrinogen Human, Human Thrombin
fibrinogen human, human thrombin
Dosage form: KIT. Category: BLA.
Cromolyn Sodium Oral Solution (concentrate)
cromolyn sodium oral solution (concentrate)
Each 5 mL ampule of Cromolyn Sodium Oral Solution (Concentrate) contains 100 mg cromolyn sodium, USP, in purified water. Cromolyn sodium is a hygroscopic, white powder having little odor. It may leave a slightly bitter aftertaste. Cromolyn Sodium Oral Solution (Concentrate) is clear, colorless, and sterile. It is intended for oral use. Chemically, cromolyn sodium is disodium 5,5’-[(2-hydroxy-trimethylene) dioxy]bis[4-oxo-4H-1-benzopyran-2-carboxylate].
Medical Disclaimer
This drug information is for educational purposes only and should not replace professional medical advice. 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.