Levofloxacin
- Product NDC
- 67296-1641
- 11-digit product format
- 672961641
- Labeler code
- 67296
- Product ID
- 67296-1641_b8d08b7b-cc02-9efd-e053-2995a90a89e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA202801
- Marketing category
- ANDA
- Marketing start
- 2019-01-01
- Marketing end
- 0000-00-00
- Substance
- LEVOFLOXACIN
- Active strength
- 250 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1641-3 | Levofloxacin | 3 in 1 BOTTLE | TABLET, FILM COATED | 3 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1641 | LEVOFLOXACIN TABLET, FILM COATED [REDPHARM DRUG, INC.] | 6 | Legacy NDC, 1 package rows | 20210114_88dedeb8-9649-5849-e053-2995a90aab72.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1641-3 | 67296164103 | 3 TABLET, FILM COATED in 1 BOTTLE (67296-1641-3) | 2019-01-01 | 0000-00-00 | No | No | Current |