NDC 68071-2383 – Ciprofloxacin
Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Coated · Oral
Product NDC68071-2383
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208921
- Marketed since
- August 12, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 250 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68071-2383-1 | 10 TABLET, COATED in 1 BOTTLE (68071-2383-1) | Apr 6, 2021 |
| 68071-2383-2 | 20 TABLET, COATED in 1 BOTTLE (68071-2383-2) | Apr 6, 2021 |
| 68071-2383-3 | 30 TABLET, COATED in 1 BOTTLE (68071-2383-3) | Apr 6, 2021 |
| 68071-2383-4 | 14 TABLET, COATED in 1 BOTTLE (68071-2383-4) | Apr 6, 2021 |
| 68071-2383-8 | 28 TABLET, COATED in 1 BOTTLE (68071-2383-8) | Apr 6, 2021 |
| 68071-2383-9 | 90 TABLET, COATED in 1 BOTTLE (68071-2383-9) | Apr 6, 2021 |
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