Ciprofloxacin
- Product NDC
- 50090-0867
- 11-digit product format
- 500900867
- Labeler code
- 50090
- Product ID
- 50090-0867_184dd943-2c06-4b68-ab73-995ef5796044
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076558
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- 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
- 2020-12-31
- 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 |
|---|
| 50090-0867-0 | 50090086700 | 6 TABLET, FILM COATED in 1 BOTTLE (50090-0867-0) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0867-1 | 50090086701 | 14 TABLET, FILM COATED in 1 BOTTLE (50090-0867-1) | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0867-2 | 50090086702 | 10 TABLET, FILM COATED in 1 BOTTLE (50090-0867-2) | 2014-11-28 | 0000-00-00 | No | No | Current |