Levofloxacin
- Product NDC
- 60760-769
- 11-digit product format
- 607600769
- Labeler code
- 60760
- Product ID
- 60760-769_46a3c5e3-b2f8-3115-e063-6394a90a1b9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA202801
- Marketing category
- ANDA
- Marketing start
- 2015-01-09
- Substance
- LEVOFLOXACIN
- Active strength
- 750 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Levofloxacin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LEVOFLOXACIN | 750 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6GNT3Y5LMF |
| Rxcui | 311296 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60760-769-10 | Levofloxacin | 10 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-769-10 | 60760076910 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-769-10) | 2025-12-23 | No | No | Current |