NDC 71205-997 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-997
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076126
- Marketed since
- October 10, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Quinolone Antimicrobial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71205-997-00 | 100 TABLET, FILM COATED in 1 BOTTLE (71205-997-00) | Mar 25, 2020 |
| 71205-997-10 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-997-10) | Mar 25, 2020 |
| 71205-997-14 | 14 TABLET, FILM COATED in 1 BOTTLE (71205-997-14) | Mar 25, 2020 |
| 71205-997-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-997-20) | Mar 25, 2020 |
| 71205-997-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-997-30) | Mar 25, 2020 |
| 71205-997-55 | 500 TABLET, FILM COATED in 1 BOTTLE (71205-997-55) | Mar 25, 2020 |
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