MOXIFLOXACIN HYDROCHLORIDE
- Product NDC
- 50090-7244
- 11-digit product format
- 500907244
- Labeler code
- 50090
- Product ID
- 50090-7244_54fdd364-609d-4d3a-8f62-8bc20bf3b74e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxifloxacin hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202632
- Marketing category
- ANDA
- Marketing start
- 2014-03-04
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MOXIFLOXACIN HYDROCHLORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MOXIFLOXACIN HYDROCHLORIDE | 400 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C53598599T |
| Rxcui | 311787 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7244-1 | MOXIFLOXACIN HYDROCHLORIDE | 7 in 1 BOTTLE | TABLET, FILM COATED | 7 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7244 | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 1 | Current NDC, 1 package rows | 20240920_02c29e8e-8346-4e28-b7fc-2f4cb61ad37d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7244-1 | 50090724401 | 7 TABLET, FILM COATED in 1 BOTTLE (50090-7244-1) | 2024-09-13 | No | No | Historical |