Ciprofloxacin
- Product NDC
- 58118-0127
- 11-digit product format
- 581180127
- Labeler code
- 58118
- Product ID
- 58118-0127_b0250bc0-31e4-fbe7-e053-2a95a90afd3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale
- 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
- 2021-12-31
- 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 |
|---|
| 58118-0127-8 | 58118012708 | 30 TABLET, FILM COATED in 1 BLISTER PACK (58118-0127-8) | 2004-06-09 | 0000-00-00 | No | No | Current |