Ciprofloxacin
- Product NDC
- 63629-8175
- 11-digit product format
- 636298175
- Labeler code
- 63629
- Product ID
- 63629-8175_0ea23e10-1a69-4ebd-808a-1e4addf1f63e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2019-07-13
- 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
- 2023-12-31
- 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 |
|---|
| 63629-8175-1 | 63629817501 | 14 TABLET, COATED in 1 BOTTLE (63629-8175-1) | 2019-07-19 | 0000-00-00 | No | No | Current |