NDC 69367-386 – Ciprofloxacin Hydrochloride
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC69367-386
Product details
- Brand name
- Ciprofloxacin Hydrochloride
- Generic name
- Ciprofloxacin Hydrochloride
- Labeler
- Westminster Pharmaceuticals, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076593
- Marketed since
- May 23, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Ciprofloxacin Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 69367-386-01 | 100 TABLET, FILM COATED in 1 BOTTLE (69367-386-01) | May 23, 2024 |
| 69367-386-05 | 500 TABLET, FILM COATED in 1 BOTTLE (69367-386-05) | May 23, 2024 |
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