Ciprofloxacin
- Product NDC
- 63629-7717
- 11-digit product format
- 636297717
- Labeler code
- 63629
- Product ID
- 63629-7717_2c2b117d-4f25-4ca3-a514-f0bc1311a2ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 63629-7717-0 | 63629771700 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-7717-0) | 2018-06-14 | 0000-00-00 | No | No | Current |
| 63629-7717-1 | 63629771701 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-7717-1) | 2018-06-14 | 0000-00-00 | No | No | Current |
| 63629-7717-2 | 63629771702 | 14 TABLET, FILM COATED in 1 BOTTLE (63629-7717-2) | 2018-06-14 | 0000-00-00 | No | No | Current |
| 63629-7717-3 | 63629771703 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-7717-3) | 2018-06-14 | 0000-00-00 | No | No | Current |
| 63629-7717-4 | 63629771704 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7717-4) | 2018-06-14 | 0000-00-00 | No | No | Current |
| 63629-7717-5 | 63629771705 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-7717-5) | 2018-06-14 | 0000-00-00 | No | No | Current |
| 63629-7717-6 | 63629771706 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-7717-6) | 2018-06-14 | 0000-00-00 | No | No | Current |
| 63629-7717-7 | 63629771707 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-7717-7) | 2018-06-14 | 0000-00-00 | No | No | Current |