NDC 63629-8357 – Moxifloxacin
Moxifloxacin Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral
Product NDC63629-8357
Product details
- Brand name
- Moxifloxacin
- Generic name
- Moxifloxacin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076938
- Marketed since
- March 5, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Moxifloxacin Hydrochloride 400 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 63629-8357-1 | 7 TABLET, FILM COATED in 1 BOTTLE (63629-8357-1) | Sep 17, 2020 |
| 63629-8357-2 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-8357-2) | Nov 5, 2020 |
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