Ciprofloxacin
- Product NDC
- 55154-2086
- 11-digit product format
- 551542086
- Labeler code
- 55154
- Product ID
- 55154-2086_bd406d48-877d-4947-af5d-576c29245b4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciprofloxacin hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076794
- Marketing category
- ANDA
- Marketing start
- 2004-08-19
- 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
- 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 |
|---|
| 55154-2086-0 | 55154208600 | 10 BLISTER PACK in 1 BAG (55154-2086-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2004-08-19 | 0000-00-00 | No | No | Current |