Glycopyrrolate
- Product NDC
- 42291-304
- 11-digit product format
- 422910304
- Labeler code
- 42291
- Product ID
- 42291-304_d57aa512-3281-7fab-e053-2a95a90aa4e6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glycopyrrolate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA090195
- Marketing category
- ANDA
- Marketing start
- 2015-05-14
- 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
- 2023-12-31
- 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 |
|---|
| 42291-304-90 | 42291030490 | 90 TABLET in 1 BOTTLE (42291-304-90) | 90 tablet | 2015-05-14 | 0000-00-00 | No | No | Current |