Vancomycin Hydrochloride
- Product NDC
- 82449-804
- 11-digit product format
- 824490804
- Labeler code
- 82449
- Product ID
- 82449-804_d53a0c06-47d4-37c6-e053-2a95a90af9e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vancomycin Hydrochloride
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- STERISCIENCE SPECIALTIES PRIVATE LIMITED
- Application
- ANDA065397
- Marketing category
- ANDA
- Marketing start
- 2013-12-05
- Marketing end
- 0000-00-00
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 1 g/20mL
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC],Glycopeptides [CS]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82449-804-02 | 82449080402 | 10 VIAL in 1 CARTON (82449-804-02) > 20 mL in 1 VIAL (82449-804-01) | 10 vial | 2013-12-05 | 0000-00-00 | No | No | Current |