VANCOMYCIN HYDROCHLORIDE
- Product NDC
- 0121-0890
- 11-digit product format
- 001210890
- Labeler code
- 0121
- Product ID
- 0121-0890_46c61b28-1b3a-4f06-bcba-bf1fba0a6287
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VANCOMYCIN HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PAI Holdings, LLC
- Application
- ANDA210729
- Marketing category
- ANDA
- Marketing start
- 2019-07-25
- Marketing end
- 0000-00-00
- Substance
- VANCOMYCIN HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Glycopeptide Antibacterial [EPC], Glycopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0121-0890 | VANCOMYCIN HYDROCHLORIDE CAPSULE [PAI HOLDINGS, LLC DBA PAI PHARMA] | 13 | Legacy NDC | 20250316_8eacc01c-5ce6-1869-e053-2a95a90a57ce.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0121-0890-20 | 00121089020 | 2 BLISTER PACK in 1 CARTON (0121-0890-20) > 10 CAPSULE in 1 BLISTER PACK | 2 blister pack | 2019-07-25 | 0000-00-00 | No | No | Current |
| 0121-0890-50 | 00121089050 | 50 CAPSULE in 1 BOTTLE (0121-0890-50) | 50 capsule | 2020-03-10 | 0000-00-00 | No | No | Current |