MOXIFLOXACIN HYDROCHLORIDE
- Product NDC
- 72789-038
- 11-digit product format
- 727890038
- Labeler code
- 72789
- Product ID
- 72789-038_4af33f79-7627-6629-e063-6294a90ad764
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxifloxacin hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA202632
- Marketing category
- ANDA
- Marketing start
- 2014-03-04
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MOXIFLOXACIN HYDROCHLORIDE
- Listing expiration
- 2027-12-31
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 |
|---|
| 72789-038-10 | MOXIFLOXACIN HYDROCHLORIDE | 10 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 10 | | 20 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-038 | MOXIFLOXACIN HYDROCHLORIDE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 18 | Current NDC, Legacy NDC, 1 package rows | 20240829_18b77b31-baf3-416f-b3b7-a631c8e46d20.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 |
|---|
| 72789-038-10 | 72789003810 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-038-10) | 2019-12-10 | 0000-00-00 | No | No | Current |