VANCOMYCIN HYDROCHLORIDE
- Product NDC
- 71467-014
- 11-digit product format
- 714670014
- Labeler code
- 71467
- Product ID
- 71467-014_0d42a289-5edd-413e-8493-67d2c0154234
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vancomycin hydrochloride
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS; ORAL
- Labeler
- Zhejiang Novus Pharma Co., Ltd.
- Application
- NDA210274
- Marketing category
- NDA
- Marketing start
- 2024-08-23
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 10.25 g/g
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC], Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- VANCOMYCIN HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VANCOMYCIN HYDROCHLORIDE | 10.25 g/g |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71467-014-01 | 71467001401 | 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (71467-014-01) / 10.25 g in 1 VIAL, PHARMACY BULK PACKAGE | 2024-08-23 | No | No | Current |