Moxifloxacin Hydrochloride
- Product NDC
- 67296-1299
- 11-digit product format
- 672961299
- Labeler code
- 67296
- Product ID
- 67296-1299_9c9f47ba-7746-719e-e053-2995a90adffe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- NDA021085
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-01-29
- 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
- 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 |
|---|
| 67296-1299-5 | Moxifloxacin Hydrochloride | 5 in 1 BOTTLE | TABLET, FILM COATED | 5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1299 | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20200122_4fd26bda-2eba-1730-e054-00144ff88e88.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 |
|---|
| 67296-1299-5 | 67296129905 | 5 TABLET, FILM COATED in 1 BOTTLE (67296-1299-5) | 2014-01-29 | 0000-00-00 | No | No | Current |