Glycopyrrolate
- Product NDC
- 68001-353
- 11-digit product format
- 680010353
- Labeler code
- 68001
- Product ID
- 68001-353_e151b061-6c47-d8ad-e053-2995a90a41e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glycopyrrolate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- BluePoint Laboratories
- Application
- ANDA208973
- Marketing category
- ANDA
- Marketing start
- 2018-04-30
- Marketing end
- 2022-08-31
- Substance
- GLYCOPYRROLATE
- Active strength
- 1 mg/5mL
- Pharmacologic classes
- Anticholinergic [EPC], Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 68001-353-72 | 68001035372 | 25 VIAL in 1 CARTON (68001-353-72) > 5 mL in 1 VIAL (68001-353-22) | 25 vial | 2018-04-30 | 2022-08-31 | No | No | Current |