Glycopyrrolate 71839-0126
Product NDC
71839-0126- 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]
Packaging Options(1)
25 VIAL, MULTI-DOSE in 1 CARTON (71839-126-25) / 20 mL in 1 VIAL, MULTI-DOSE (71839-126-01)