GLYCOPYRROLATE
- Product NDC
- 70518-3152
- 11-digit product format
- 705183152
- Labeler code
- 70518
- Product ID
- 70518-3152_ee50706a-c9b9-e353-e053-2995a90a82eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLYCOPYRROLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091182
- Marketing category
- ANDA
- Marketing start
- 2021-07-14
- 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 |
|---|
| 70518-3152-0 | 70518315200 | 100 POUCH in 1 BOX (70518-3152-0) > 1 TABLET in 1 POUCH (70518-3152-1) | 100 pouch | 2021-07-14 | 0000-00-00 | No | No | Current |