72789-080 : Moxifloxacin Hydrochloride Tablets, 400 mg 400 mg Oral Tablet, Film Coated
| NDC: | 72789-080 |
| Labeler: | Pd-rx Pharmaceuticals, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Moxifloxacin Hydrochloride Tablets, 400 mg |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | ANDA208682 |
| Rev. Date: |
Appearance:
| Markings: | M;400 |
| Shapes: |
Capsule |
| Colors: |
 Red |
| Size (mm): | 17 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
NDC Package Codes:
- 72789-080-10: 10 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (72789‑080‑10)
Active Ingredients:
- Moxifloxacin Hydrochloride Monohydrate
Dosage Strength:
- 400 mg
Inactive Ingredients:
- Lactose Monohydrate
- Povidone K30
- Anhydrous Lactose
- Croscarmellose Sodium
- Silicon Dioxide
- Magnesium Stearate
- Titanium Dioxide
- Hypromelloses
- Polyethylene Glycol 400
- Ferric Oxide Red /
Pharmaceutical Classes:
- Quinolone Antimicrobial [EPC]
- Quinolones [CS]
Related Products:
Based on records with the same trade name.- 69539-006 Moxifloxacin Hydrochloride Tablets, 400 mg 400 mg Oral Tablet, Film Coated by Msn Laboratories Private Limited
- 72205-001 Moxifloxacin Hydrochloride Tablets, 400 mg 400 mg Oral Tablet, Film Coated by Novadoz Pharmaceuticals LLC
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.