Glycopyrrolate
- Product NDC
- 71872-7179
- 11-digit product format
- 718727179
- Labeler code
- 71872
- Product ID
- 71872-7179_fbbcf473-155c-8551-e053-6294a90af96d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glycopyrrolate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA211334
- Marketing category
- ANDA
- Marketing start
- 2019-07-22
- Substance
- GLYCOPYRROLATE
- Active strength
- 4 mg/20mL
- 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 |
|---|
| 71872-7179-1 | 71872717901 | 1 VIAL in 1 BAG (71872-7179-1) / 20 mL in 1 VIAL | 1 vial | 2019-10-01 | No | No | Historical |