NDC 59651-978 – Ciprofloxacin
Ciprofloxacin Hydrochloride 750 mg/1 · Tablet, Film Coated · Oral
Product NDC59651-978
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077859
- Marketed since
- March 27, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 750 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 59651-978-01 | 100 TABLET, FILM COATED in 1 BOTTLE (59651-978-01) | Mar 27, 2025 |
| 59651-978-05 | 500 TABLET, FILM COATED in 1 BOTTLE (59651-978-05) | Mar 27, 2025 |
| 59651-978-20 | 20 TABLET, FILM COATED in 1 BOTTLE (59651-978-20) | Mar 27, 2025 |
| 59651-978-50 | 50 TABLET, FILM COATED in 1 BOTTLE (59651-978-50) | Mar 27, 2025 |
| 59651-978-98 | 1000 TABLET, FILM COATED in 1 BOTTLE (59651-978-98) | Mar 27, 2025 |
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