NDC 51655-086 – Ciprofloxacin
Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-086
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076558
- Marketed since
- March 1, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 250 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51655-086-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-086-20) | Jun 22, 2023 |
| 51655-086-84 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-086-84) | Mar 1, 2023 |
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