Ciprofloxacin
- Product NDC
- 68788-9228
- 11-digit product format
- 687889228
- Labeler code
- 68788
- Product ID
- 68788-9228_dde1647f-0a39-4cb1-9e42-ac59b0dc2a91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2014-11-12
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record