NDC 16571-412 – ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC16571-412
Product details
- Brand name
- ciprofloxacin
- Generic name
- ciprofloxacin
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076639
- Marketed since
- September 10, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 16571-412-10 | 100 TABLET, FILM COATED in 1 BOTTLE (16571-412-10) | Sep 10, 2004 |
| 16571-412-50 | 500 TABLET, FILM COATED in 1 BOTTLE (16571-412-50) | Sep 10, 2004 |
Recalls mentioning this NDC
- D-1422-2012 Jul 25, 2012 · Class III
Labeling Illegible: Missing Label; The voluntary recall of the aforementioned batch of product is being initiated due to two bottles missing container labels.
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