ciprofloxacin
- Product NDC
- 50090-2265
- 11-digit product format
- 500902265
- Labeler code
- 50090
- Product ID
- 50090-2265_774c4d63-d6e5-479f-81f2-df7b3fc86140
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciprofloxacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076639
- Marketing category
- ANDA
- Marketing start
- 2004-09-10
- 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