Ciprofloxacin
- Product NDC
- 50090-3130
- 11-digit product format
- 500903130
- Labeler code
- 50090
- Product ID
- 50090-3130_83ef532d-2288-41d9-b8a0-2f753d07a45c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076126
- Marketing category
- ANDA
- Marketing start
- 2009-10-10
- 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
- 2021-12-31
- 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 |
|---|
| 50090-3130-0 | 50090313000 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-3130-0) | 2017-09-05 | 0000-00-00 | No | No | Current |