NDC 70518-3738 – Moxifloxacin Hydrochloride
Moxifloxacin Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-3738
Product details
- Brand name
- Moxifloxacin Hydrochloride
- Generic name
- Moxifloxacin hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202632
- Marketed since
- May 30, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Moxifloxacin Hydrochloride 400 mg/1
Uses, dosage, side effects and warnings for Moxifloxacin Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3738-0 | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3738-0) | May 30, 2023 |
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