NDC 73473-903 – Moxifloxacin
Moxifloxacin Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral
Product NDC73473-903
Product details
- Brand name
- Moxifloxacin
- Generic name
- Moxifloxacin hydrochloride
- Labeler
- Solaris Pharma Corporation
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206295
- Marketed since
- December 12, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Moxifloxacin Hydrochloride 400 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 73473-903-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73473-903-30) | Dec 12, 2025 |
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