Moxifloxacin Hydrochloride
- Product NDC
- 50090-4100
- 11-digit product format
- 500904100
- Labeler code
- 50090
- Product ID
- 50090-4100_71560b50-ebf3-47e9-a940-9daa58967490
- 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 |
|---|
| 50090-4100 | MOXIFLOXACIN HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 9 | Legacy NDC | 20250108_f596ed10-197c-4c27-a1fa-9a399bdefdfa.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4100-0 | 50090410000 | 10 TABLET in 1 BOTTLE (50090-4100-0) | 10 tablet | 2019-01-25 | 0000-00-00 | No | No | Current |