Glycopyrrolate
- Product NDC
- 71335-0020
- 11-digit product format
- 713350020
- Labeler code
- 71335
- Product ID
- 71335-0020_f4acfa41-26f3-4dc0-8be5-d3d7230bace0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glycopyrrolate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090195
- Marketing category
- ANDA
- Marketing start
- 2018-09-22
- 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 |
|---|
| 71335-0020-1 | 71335002001 | 30 TABLET in 1 BOTTLE (71335-0020-1) | 30 tablet | 2018-09-22 | 0000-00-00 | No | No | Current |
| 71335-0020-2 | 71335002002 | 90 TABLET in 1 BOTTLE (71335-0020-2) | 90 tablet | 2018-09-22 | 0000-00-00 | No | No | Current |
| 71335-0020-3 | 71335002003 | 28 TABLET in 1 BOTTLE (71335-0020-3) | 28 tablet | 2018-09-22 | 0000-00-00 | No | No | Current |
| 71335-0020-4 | 71335002004 | 18 TABLET in 1 BOTTLE (71335-0020-4) | 18 tablet | 2018-09-22 | 0000-00-00 | No | No | Current |