Glycopyrrolate 71839-0124

Product NDC

71839-0124

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/2mL

Drug Class

Anticholinergic [EPC]Cholinergic Antagonists [MoA]

Packaging Options(1)

71839-0124-25

25 VIAL, SINGLE-DOSE in 1 CARTON (71839-124-25) / 2 mL in 1 VIAL, SINGLE-DOSE (71839-124-01)

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