Moxifloxacin Hydrochloride
- Product NDC
- 50090-4058
- 11-digit product format
- 500904058
- Labeler code
- 50090
- Product ID
- 50090-4058_0a285b71-8acc-438f-bcfd-1b67610599af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA205348
- Marketing category
- ANDA
- Marketing start
- 2017-05-02
- Marketing end
- 0000-00-00
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4058 | MOXIFLOXACIN HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 9 | Legacy NDC | 20250108_4971357a-13b8-4f0a-a314-ed05b9fd7c18.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4058-1 | 50090405801 | 30 TABLET in 1 BOTTLE (50090-4058-1) | 30 tablet | 2019-01-15 | 0000-00-00 | No | No | Current |