Ciprofloxacin
- Product NDC
- 50090-5371
- 11-digit product format
- 500905371
- Labeler code
- 50090
- Product ID
- 50090-5371_1c4c8542-d1e7-4c44-b572-151a9bcf5099
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2007-04-26
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5371-0 | 50090537100 | 6 TABLET, FILM COATED in 1 BOTTLE (50090-5371-0) | 2020-11-18 | 0000-00-00 | No | No | Current |
| 50090-5371-1 | 50090537101 | 14 TABLET, FILM COATED in 1 BOTTLE (50090-5371-1) | 2020-11-18 | 0000-00-00 | No | No | Current |