Glycopyrrolate 71839-0126-25

Package NDC

71839-0126-25

Manufacturer: Be Pharmaceuticals Inc.
Dosage Form: Injection
Route: Intramuscular And Intravenous
Product Type: Human Prescription Drug
Marketing Start: March 10, 2022
Listing Expires: December 31, 2026
Application: ANDA211705

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Active Ingredients

Ingredient	Strength
Glycopyrrolate	4 mg/20mL

Drug Class

Anticholinergic [EPC]Cholinergic Antagonists [MoA]

Selected Package

71839-0126-25Selected

25 VIAL, MULTI-DOSE in 1 CARTON (71839-126-25) / 20 mL in 1 VIAL, MULTI-DOSE (71839-126-01)