NDC 50419-754 – Cipro
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC50419-754
Product details
- Brand name
- Cipro
- Generic name
- ciprofloxacin hydrochloride
- Labeler
- Bayer HealthCare Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA · NDA019537
- Marketed since
- October 22, 1987
- Listing expires
- December 31, 2027
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 50419-754-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-754-01) | Oct 22, 1987 |
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