NDC 69117-0009 – Ciprofloxacin
Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Coated · Oral
Product NDC69117-0009
Product details
- Brand name
- Ciprofloxacin
- Generic name
- Ciprofloxacin Tablets
- Labeler
- Yiling Pharmaceutical, Inc.
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208921
- Marketed since
- July 13, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Ciprofloxacin Hydrochloride 500 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 69117-0009-1 | 500 TABLET, COATED in 1 BOTTLE (69117-0009-1) | Jul 13, 2019 |
| 69117-0009-2 | 100 TABLET, COATED in 1 BOTTLE (69117-0009-2) | Jul 13, 2019 |
Other Ciprofloxacin products
- 71335-2097 Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Coated · Bryant Ranch Prepack
- 71335-1229 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Coated · Bryant Ranch Prepack
- 71335-1152 Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Coated · Bryant Ranch Prepack
- 71335-2054 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Coated · Bryant Ranch Prepack
- 72189-323 Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Coated · Direct Rx
- 58657-676 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Coated · Method Pharmaceuticals, LLC
- 58657-675 Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Coated · Method Pharmaceuticals, LLC
- 51655-490 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Coated · Northwind Health Company, LLC
- 68071-2384 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Coated · NuCare Pharmaceuticals,Inc.
- 68071-2404 Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Coated · NuCare Pharmaceuticals,Inc.
- 68071-2383 Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Coated · NuCare Pharmaceuticals,Inc.
- 68788-8200 Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Coated · Preferred Pharmaceuticals Inc.