Glycopyrrolate
- Product NDC
- 60687-270
- 11-digit product format
- 606870270
- Labeler code
- 60687
- Product ID
- 60687-270_84eb2e6d-7073-cca9-e053-2991aa0a5ad7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glycopyrrolate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA040653
- Marketing category
- ANDA
- Marketing start
- 2017-05-24
- Marketing end
- 2020-07-31
- Substance
- GLYCOPYRROLATE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record