GLYCOPYRROLATE
- Product NDC
- 71872-7208
- 11-digit product format
- 718727208
- Labeler code
- 71872
- Product ID
- 71872-7208_fad2cfd6-08a1-a491-e053-6394a90a5043
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glycopyrrolate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA210927
- Marketing category
- ANDA
- Marketing start
- 2019-03-20
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7208-1 | 71872720801 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7208-1) / 1 mL in 1 VIAL, SINGLE-DOSE | 2020-03-30 | No | No | Historical |