vancomycin hydrochloride
- Product NDC
- 47781-729
- 11-digit product format
- 477810729
- Labeler code
- 47781
- Product ID
- 47781-729_41dd88a2-d5df-8c34-e9f8-2dd4bac6d5d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vancomycin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Alvogen Inc.
- Application
- ANDA065490
- Marketing category
- ANDA
- Marketing start
- 2012-04-09
- Marketing end
- 0000-00-00
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 125 mg/1
- 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 |
|---|
| 47781-729-02 | 47781072902 | 2 BLISTER PACK in 1 CARTON (47781-729-02) > 10 CAPSULE in 1 BLISTER PACK | 2 blister pack | 2012-04-09 | 0000-00-00 | No | No | Current |
| 47781-729-50 | 47781072950 | 50 CAPSULE in 1 BOTTLE (47781-729-50) | 50 capsule | 2012-04-09 | 0000-00-00 | No | No | Current |