Glycopyrrolate
- Product NDC
- 69067-050
- 11-digit product format
- 690670050
- Labeler code
- 69067
- Product ID
- 69067-050_0bb70b28-bf45-4cc6-b64f-91b94c1eb0ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLYCOPYRROLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Foxland Pharmaceuticals, Inc.
- Application
- ANDA091522
- Marketing category
- ANDA
- Marketing start
- 2018-10-10
- Marketing end
- 0000-00-00
- Substance
- GLYCOPYRROLATE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69067-050-30 | 69067005030 | 30 TABLET in 1 BOTTLE (69067-050-30) | 30 tablet | 2018-10-10 | 0000-00-00 | No | No | Current |