Ciprofloxacin
- Product NDC
- 16714-653
- 11-digit product format
- 167140653
- Labeler code
- 16714
- Product ID
- 16714-653_f6e904df-0c07-4985-a018-d0e71bc04cfc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2007-04-26
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 750 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 |
|---|
| 16714-653-01 | 16714065301 | 50 TABLET, FILM COATED in 1 BOTTLE (16714-653-01) | 2007-04-26 | 0000-00-00 | No | No | Current |