Ciprofloxacin
- Product NDC
- 63629-7648
- 11-digit product format
- 636297648
- Labeler code
- 63629
- Product ID
- 63629-7648_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
- 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 |
|---|
| 63629-7648-1 | 63629764801 | 14 TABLET, FILM COATED in 1 BOTTLE (63629-7648-1) | 2012-09-05 | 0000-00-00 | No | No | Current |
| 63629-7648-2 | 63629764802 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-7648-2) | 2012-09-05 | 0000-00-00 | No | No | Current |
| 63629-7648-3 | 63629764803 | 40 TABLET, FILM COATED in 1 BOTTLE (63629-7648-3) | 2012-09-05 | 0000-00-00 | No | No | Current |
| 63629-7648-4 | 63629764804 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-7648-4) | 2012-09-05 | 0000-00-00 | No | No | Current |