Ciprofloxacin
- Product NDC
- 63629-6360
- 11-digit product format
- 636296360
- Labeler code
- 63629
- Product ID
- 63629-6360_6db6de12-1cb4-4165-9267-611a3fde6446
- 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
- 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 |
|---|
| 63629-6360-1 | 63629636001 | 14 TABLET, FILM COATED in 1 BOTTLE (63629-6360-1) | 2015-09-04 | 0000-00-00 | No | No | Current |
| 63629-6360-2 | 63629636002 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-6360-2) | 2015-09-09 | 0000-00-00 | No | No | Current |
| 63629-6360-3 | 63629636003 | 28 TABLET, FILM COATED in 1 BOTTLE (63629-6360-3) | 2015-09-09 | 0000-00-00 | No | No | Current |
| 63629-6360-4 | 63629636004 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-6360-4) | 2016-01-21 | 0000-00-00 | No | No | Current |