Ciprofloxacin
- Product NDC
- 60760-074
- 11-digit product format
- 607600074
- Labeler code
- 60760
- Product ID
- 60760-074_b69a3586-03d4-60cd-e053-2a95a90a00d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- St Mary's Medical Park Pharmacy
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- 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 |
|---|
| 60760-074-10 | 60760007410 | 10 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-074-10) | 2019-03-12 | 0000-00-00 | No | No | Current |
| 60760-074-20 | 60760007420 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-074-20) | 2019-11-21 | 0000-00-00 | No | No | Current |