ciprofloxacin
- Product NDC
- 50090-3160
- 11-digit product format
- 500903160
- Labeler code
- 50090
- Product ID
- 50090-3160_54aa3131-0bd6-4e65-8dd5-854d09dcb821
- 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
- 250 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3160-0 | 50090316000 | 6 TABLET in 1 BOTTLE (50090-3160-0) | 6 tablet | 2017-10-30 | 0000-00-00 | No | No | Current |
| 50090-3160-1 | 50090316001 | 14 TABLET in 1 BOTTLE (50090-3160-1) | 14 tablet | 2017-12-05 | 0000-00-00 | No | No | Current |
| 50090-3160-2 | 50090316002 | 10 TABLET in 1 BOTTLE (50090-3160-2) | 10 tablet | 2017-10-10 | 0000-00-00 | No | No | Current |