Glycopyrrolate
- Product NDC
- 71872-7237
- 11-digit product format
- 718727237
- Labeler code
- 71872
- Product ID
- 71872-7237_fae6fad6-a46d-1ae8-e053-6394a90a4a97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glycopyrrolate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA210246
- Marketing category
- ANDA
- Marketing start
- 2020-06-10
- Substance
- GLYCOPYRROLATE
- Active strength
- .2 mg/mL
- Pharmacologic classes
- Anticholinergic [EPC], Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| V92SO9WP2I | GLYCOPYRROLATE | 51186-83-5 | GLYCOPYRROLATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7237-1 | 71872723701 | 1 VIAL in 1 BAG (71872-7237-1) / 20 mL in 1 VIAL | 1 vial | 2021-01-28 | No | No | Historical |