Ciprofloxacin
- Product NDC
- 42291-219
- 11-digit product format
- 422910219
- Labeler code
- 42291
- Product ID
- 42291-219_d579f9b1-384f-52b6-e053-2a95a90a93f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA076126
- Marketing category
- ANDA
- Marketing start
- 2014-06-17
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-219-01 | 42291021901 | 100 TABLET, FILM COATED in 1 BOTTLE (42291-219-01) | 2014-06-17 | 0000-00-00 | No | No | Current |