NDC 70518-4312 – Moxifloxacin Hydrochloride Tablets, 400 mg
Moxifloxacin Hydrochloride Monohydrate 400 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-4312
Product details
- Brand name
- Moxifloxacin Hydrochloride Tablets, 400 mg
- Generic name
- Moxifloxacin Hydrochloride Tablets, 400 mg
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208682
- Marketed since
- March 18, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
Uses, dosage, side effects and warnings for Moxifloxacin Hydrochloride Tablets, 400 mg →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4312-0 | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4312-0) | Mar 18, 2025 |