Levofloxacin
- Product NDC
- 70934-738
- 11-digit product format
- 709340738
- Labeler code
- 70934
- Product ID
- 70934-738_a9cc64f6-5701-22b7-e053-2a95a90a2259
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA077438
- Marketing category
- ANDA
- Marketing start
- 2020-05-26
- Marketing end
- 0000-00-00
- Substance
- LEVOFLOXACIN
- Active strength
- 750 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70934-738-05 | Levofloxacin | 5 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 5 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70934-738 | LEVOFLOXACIN TABLET, FILM COATED [DENTON PHARMA, INC. DBA NORTHWIND PHARMACEUTICALS] | 1 | Legacy NDC, 1 package rows | 20201106_a9cc7f89-153b-25db-e053-2a95a90ad662.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 |
|---|
| 70934-738-05 | 70934073805 | 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-738-05) | 2020-05-26 | 0000-00-00 | No | No | Current |