Vancomycin Hydrochloride
- Product NDC
- 72162-2305
- 11-digit product format
- 721622305
- Labeler code
- 72162
- Product ID
- 72162-2305_38c75f1c-f29c-4671-aa99-f9d3f7c650ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vancomycin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210729
- Marketing category
- ANDA
- Marketing start
- 2024-01-15
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 125 mg/1
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC], Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 71WO621TJD | VANCOMYCIN HYDROCHLORIDE | 1404-93-9 | VANCOMYCIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2305-4 | 72162230504 | 50 CAPSULE in 1 BOTTLE (72162-2305-4) | 50 capsule | 2024-05-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Vancomycin Hydrochloride | Bryant Ranch Prepack | 2024-05-13 | HUMAN PRESCRIPTION DRUG LABEL | 100 |