Vancomycin Hydrochloride
- Product NDC
- 51991-940
- 11-digit product format
- 519910940
- Labeler code
- 51991
- Product ID
- 51991-940_d5cc977d-305b-46da-ae64-d8351426886b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vancomycin
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Application
- ANDA205694
- Marketing category
- ANDA
- Marketing start
- 2016-02-23
- Marketing end
- 2021-04-30
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC],Glycopeptides [CS]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51991-940-17 | 51991094017 | 10 VIAL, SINGLE-USE in 1 CARTON (51991-940-17) > 1 INJECTION, SOLUTION in 1 VIAL, SINGLE-USE (51991-940-99) | 2017-04-28 | 2021-04-30 | No | No | Current |