Ciprofloxacin
- Product NDC
- 70934-480
- 11-digit product format
- 709340480
- Labeler code
- 70934
- Product ID
- 70934-480_d244f832-8930-484c-e053-2995a90ac3ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2020-01-15
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-480-06 | 70934048006 | 6 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-480-06) | 2020-01-15 | 0000-00-00 | No | No | Current |
| 70934-480-14 | 70934048014 | 14 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-480-14) | 2020-01-15 | 0000-00-00 | No | No | Current |
| 70934-480-20 | 70934048020 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-480-20) | 2020-01-15 | 0000-00-00 | No | No | Current |