NDC 51655-490 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Coated · Oral
Product NDC51655-490
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208921
- Marketed since
- January 5, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 51655-490-20 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-20) | Feb 3, 2023 |
| 51655-490-52 | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-52) | Jan 5, 2023 |
| 51655-490-53 | 10 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-53) | Feb 3, 2023 |
| 51655-490-84 | 14 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-84) | Jan 20, 2023 |
| 51655-490-87 | 6 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-87) | Jan 5, 2023 |
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