Ciprofloxacin
- Product NDC
- 63629-2311
- 11-digit product format
- 636292311
- Labeler code
- 63629
- Product ID
- 63629-2311_de736b6a-054e-4223-bc41-e6bc9b943bbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2020-08-12
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2311-1 | 63629231101 | 100 TABLET, COATED in 1 BOTTLE (63629-2311-1) | 2021-02-17 | 0000-00-00 | No | No | Current |