NDC 67296-2291 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC67296-2291
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Redpharm Drug
- 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 500 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 67296-2291-4 | 14 TABLET, FILM COATED in 1 BOTTLE (67296-2291-4) | Mar 27, 2025 |
Other ciprofloxacin products
- 50090-7297 Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · A-S Medication Solutions
- 50090-7581 Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-4600 Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-1648 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · A-S Medication Solutions
- 50090-3791 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-5373 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-4217 Ciprofloxacin Hydrochloride 3 mg/mL · Solution · A-S Medication Solutions
- 50090-3852 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-2146 Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-1649 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · A-S Medication Solutions
- 80425-0492 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Advanced Rx of Tennessee, LLC
- 80425-0499 Ciprofloxacin Hydrochloride 3 mg/mL · Solution · Advanced Rx of Tennessee, LLC