ciprofloxacin
- Product NDC
- 60687-539
- 11-digit product format
- 606870539
- Labeler code
- 60687
- Product ID
- 60687-539_a13a0cb6-723a-319b-e053-2995a90af537
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciprofloxacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA076639
- Marketing category
- ANDA
- Marketing start
- 2020-03-19
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-539-01 | 60687053901 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-539-01) > 1 TABLET in 1 BLISTER PACK (60687-539-11) | 100 blister pack | 2020-03-19 | 0000-00-00 | No | No | Current |