GLYCOPYRROLATE
- Product NDC
- 50742-488
- 11-digit product format
- 507420488
- Labeler code
- 50742
- Product ID
- 50742-488_8cb72674-1c75-4138-affb-9070e3b23817
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glycopyrrolate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA210083
- Marketing category
- ANDA
- Marketing start
- 2020-02-20
- Marketing end
- 0000-00-00
- Substance
- GLYCOPYRROLATE
- Active strength
- 1 mg/5mL
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 50742-488-06 | 50742048806 | 25 VIAL in 1 CARTON (50742-488-06) > 5 mL in 1 VIAL (50742-488-05) | 25 vial | 2020-02-20 | 0000-00-00 | No | No | Current |