Ciprofloxacin
- Product NDC
- 63629-6358
- 11-digit product format
- 636296358
- Labeler code
- 63629
- Product ID
- 63629-6358_b621182d-a516-43a6-92e3-7ab7d9f5f503
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075593
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- 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
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 |
|---|
| 63629-6358-1 | 63629635801 | 14 TABLET, FILM COATED in 1 BOTTLE (63629-6358-1) | 2015-09-04 | 0000-00-00 | No | No | Current |
| 63629-6358-2 | 63629635802 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-6358-2) | 2015-10-15 | 0000-00-00 | No | No | Current |
| 63629-6358-3 | 63629635803 | 6 TABLET, FILM COATED in 1 BOTTLE (63629-6358-3) | 2016-05-20 | 0000-00-00 | No | No | Current |