NDC 31722-845 – Moxifloxacin
Moxifloxacin Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-845
Product details
- Brand name
- Moxifloxacin
- Generic name
- Moxifloxacin
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204836
- Marketed since
- March 2, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Moxifloxacin Hydrochloride 400 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 31722-845-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-845-05) | Mar 2, 2023 |
| 31722-845-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-845-30) | Mar 2, 2023 |
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