NDC 61442-222 – Ciprofloxacin
Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Film Coated · Oral
Product NDC61442-222
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Carlsbad Technology, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076126
- Marketed since
- October 10, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 250 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 61442-222-01 | 100 TABLET, FILM COATED in 1 BOTTLE (61442-222-01) | Oct 10, 2009 |
| 61442-222-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (61442-222-10) | Oct 10, 2009 |
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