Avelox
- Product NDC
- 67296-0154
- 11-digit product format
- 672960154
- Labeler code
- 67296
- Product ID
- 67296-0154_4c8fe3c9-0537-4fda-aef5-918f0a961a8b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxifloxacin hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug Inc.
- Application
- NDA021085
- Marketing category
- NDA
- Marketing start
- 2011-02-25
- Marketing end
- 0000-00-00
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 67296-0154-1 | Avelox | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | | 2 |
| 67296-0154-2 | Avelox | 7 in 1 BOTTLE | TABLET, FILM COATED | 7 | | 2 |
| 67296-0154-3 | Avelox | 5 in 1 BOTTLE | TABLET, FILM COATED | 5 | | 2 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| MOXIFLOXACIN HYDROCHLORIDE | ACTIVE INGREDIENT | C53598599T | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | |
| MOXIFLOXACIN | ACTIVE MOIETY | U188XYD42P | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | |
| POLYETHYLENE GLYCOL | INACTIVE INGREDIENT | 3WJQ0SDW1A | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0154 | AVELOX (MOXIFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [REDPHARM DRUG INC.] | 2 | Legacy NDC, 3 package rows | 20110815_fe9226f8-64f4-4eff-8339-ed3fce0896f2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67296-0154-1 | 67296015401 | 10 in 1 BOTTLE | Historical |
| 67296-0154-2 | 67296015402 | 7 in 1 BOTTLE | Historical |
| 67296-0154-3 | 67296015403 | 5 in 1 BOTTLE | Historical |