NDC 76420-214 – Ciprofloxacin
Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Film Coated · Oral
Product NDC76420-214
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin
- Labeler
- Asclemed USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076558
- Marketed since
- June 9, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Quinolone Antimicrobial
Active ingredients
- Ciprofloxacin Hydrochloride 250 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 76420-214-06 | 6 TABLET, FILM COATED in 1 BOTTLE (76420-214-06) | Mar 8, 2022 |
| 76420-214-10 | 10 TABLET, FILM COATED in 1 BOTTLE (76420-214-10) | Mar 8, 2022 |
| 76420-214-14 | 14 TABLET, FILM COATED in 1 BOTTLE (76420-214-14) | Mar 8, 2022 |
| 76420-214-20 | 20 TABLET, FILM COATED in 1 BOTTLE (76420-214-20) | Mar 8, 2022 |
| 76420-214-30 | 30 TABLET, FILM COATED in 1 BOTTLE (76420-214-30) | Mar 8, 2022 |
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