Moxifloxacin Hydrochloride
- Product NDC
- 68084-722
- 11-digit product format
- 680840722
- Labeler code
- 68084
- Product ID
- 68084-722_2b24dadc-fe4e-61dd-e063-6294a90a2a96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA202632
- Marketing category
- ANDA
- Marketing start
- 2014-03-19
- 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 |
|---|
| 68084-722-11 | Moxifloxacin Hydrochloride | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 10 |
| 68084-722-65 | Moxifloxacin Hydrochloride | 50 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 50 | | 10 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| MOXIFLOXACIN HYDROCHLORIDE | ACTIVE INGREDIENT | C53598599T | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 1 | |
| MOXIFLOXACIN | ACTIVE MOIETY | U188XYD42P | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 1 | |
| HYPROMELLOSE 2910 (6 MPA.S) | INACTIVE INGREDIENT | 0WZ8WG20P6 | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 1 | |
| POLYETHYLENE GLYCOL 4000 | INACTIVE INGREDIENT | 4R4HFI6D95 | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 1 | |
| POVIDONE K30 | INACTIVE INGREDIENT | U725QWY32X | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68084-722 | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 10 | Current NDC, Legacy NDC, 2 package rows | 20250109_1ed191f5-7df5-488c-bb72-91ac0b618d9a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-722-11 | 68084072211 | 1 in 1 BLISTER PACK | | | | | | Historical |
| 68084-722-65 | 68084072265 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11) | 50 blister pack | 2014-03-19 | 0000-00-00 | No | No | Current |