Glycopyrrolate
- Product NDC
- 16714-998
- 11-digit product format
- 167140998
- Labeler code
- 16714
- Product ID
- 16714-998_3eaeb69f-49ab-4d30-936a-897970b311da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glycopyrrolate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- NorthStar Rx LLC
- Application
- ANDA211705
- Marketing category
- ANDA
- Marketing start
- 2019-05-15
- Marketing end
- 0000-00-00
- Substance
- GLYCOPYRROLATE
- Active strength
- 0 mg/mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-998-25 | 16714099825 | 25 VIAL, SINGLE-DOSE in 1 CARTON (16714-998-25) > 2 mL in 1 VIAL, SINGLE-DOSE (16714-998-01) | 2019-05-15 | 2023-01-31 | No | No | Current |