NDC 68084-722 – Moxifloxacin Hydrochloride
Moxifloxacin Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral
Product NDC68084-722
Product details
- Brand name
- Moxifloxacin Hydrochloride
- Generic name
- Moxifloxacin Hydrochloride
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202632
- Marketed since
- March 19, 2014
- 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 |
|---|---|---|
| 68084-722-65 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11) | Mar 19, 2014 |
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