NDC 33342-322 – Moxifloxacin
Moxifloxacin Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral
Product NDC33342-322
Product details
- Brand name
- Moxifloxacin
- Generic name
- Moxifloxacin
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209143
- Marketed since
- March 2, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Moxifloxacin Hydrochloride 400 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 33342-322-07 | 30 TABLET, FILM COATED in 1 BOTTLE (33342-322-07) | Mar 2, 2026 |
| 33342-322-12 | 10 BLISTER PACK in 1 CARTON (33342-322-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Mar 2, 2026 |
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