48792-7823 : Moxifloxacin 400 mg Oral Tablet, Film Coated
| NDC: | 48792-7823 |
| Labeler: | Sunshine Lake Pharma Co., Ltd. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Moxifloxacin |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | ANDA206295 |
| Rev. Date: |
Appearance:
| Markings: | S9 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 19 |
| 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:
- 48792-7823-1: 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (48792‑7823‑1)
Active Ingredients:
- Moxifloxacin Hydrochloride
Dosage Strength:
- 400 mg
Inactive Ingredients:
- Cellulose, Microcrystalline
- Mannitol
- Croscarmellose Sodium
- Magnesium Stearate
- Hypromelloses
- Titanium Dioxide
- Polyethylene Glycol, Unspecified /
Pharmaceutical Classes:
- Quinolone Antimicrobial [EPC]
- Quinolones [CS]
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- 55700-638 Moxifloxacin 400 mg Oral Tablet, Film Coated by Lake Erie Medical Dba Quality Care Products LLC
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- 60505-0582 Moxifloxacin 5 mg/ml Ophthalmic Solution/ Drops by Apotex Corp.
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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.