Ciprofloxacin
- Product NDC
- 50090-5621
- 11-digit product format
- 500905621
- Labeler code
- 50090
- Product ID
- 50090-5621_044d3de8-7717-47c8-9d16-a4675e0d6de4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075593
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- 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
- 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 |
|---|
| 50090-5621-0 | 50090562100 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-5621-0) | 2021-08-26 | 0000-00-00 | No | No | Current |
| 50090-5621-1 | 50090562101 | 14 TABLET, FILM COATED in 1 BOTTLE (50090-5621-1) | 2021-08-26 | 0000-00-00 | No | No | Current |
| 50090-5621-3 | 50090562103 | 6 TABLET, FILM COATED in 1 BOTTLE (50090-5621-3) | 2021-08-26 | 0000-00-00 | No | No | Current |
| 50090-5621-4 | 50090562104 | 28 TABLET, FILM COATED in 1 BOTTLE (50090-5621-4) | 2021-08-26 | 0000-00-00 | No | No | Current |
| 50090-5621-5 | 50090562105 | 10 TABLET, FILM COATED in 1 BOTTLE (50090-5621-5) | 2021-08-26 | 0000-00-00 | No | No | Current |
| 50090-5621-7 | 50090562107 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-5621-7) | 2021-08-26 | 0000-00-00 | No | No | Current |
| 50090-5621-8 | 50090562108 | 1 TABLET, FILM COATED in 1 BOTTLE (50090-5621-8) | 2021-08-26 | 0000-00-00 | No | No | Current |