Vancomycin Hydrochloride
- Product NDC
- 17478-742
- 11-digit product format
- 174780742
- Labeler code
- 17478
- Product ID
- 17478-742_179de172-3fc5-448d-876b-e4fd6fc166d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vancomycin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Akorn
- Application
- ANDA065478
- Marketing category
- ANDA
- Marketing start
- 2012-04-09
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17478-742 | VANCOMYCIN HYDROCHLORIDE CAPSULE [AKORN] | 14 | Legacy NDC | 20221220_0e7ead22-9618-418f-85a1-4d5ed0949f78.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-742-02 | 17478074202 | 2 BLISTER PACK in 1 CARTON (17478-742-02) > 10 CAPSULE in 1 BLISTER PACK | 2 blister pack | 2012-04-09 | 0000-00-00 | No | No | Current |