Glycopyrrolate
- Product NDC
- 0904-6521
- 11-digit product format
- 009046521
- Labeler code
- 0904
- Product ID
- 0904-6521_b7ad3b08-48a4-486a-a2d7-960104d6af34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glycopyrrolate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA090195
- Marketing category
- ANDA
- Marketing start
- 2016-03-18
- Marketing end
- 0000-00-00
- Substance
- GLYCOPYRROLATE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record