GLYCOPYRROLATE
- Product NDC
- 52584-679
- 11-digit product format
- 525840679
- Labeler code
- 52584
- Product ID
- 52584-679_c4e97264-4f50-47e7-8f6d-11280ab83820
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLYCOPYRROLATE
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA090963
- Marketing category
- ANDA
- Marketing start
- 2018-07-02
- Marketing end
- 2023-02-28
- Substance
- GLYCOPYRROLATE
- Active strength
- 0 mg/mL
- 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 |
|---|
| 52584-679-01 | 52584067901 | 1 VIAL in 1 BAG (52584-679-01) > 20 mL in 1 VIAL | 1 vial | 2018-07-02 | 0000-00-00 | No | No | Current |