Ciprofloxacin
- Product NDC
- 55154-8148
- 11-digit product format
- 551548148
- Labeler code
- 55154
- Product ID
- 55154-8148_3fb18711-3c17-419a-bddc-a08a502e96e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2007-04-26
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4BA73M5E37 | CIPROFLOXACIN HYDROCHLORIDE | 86393-32-0 | CIPROFLOXACIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-8148-0 | 55154814800 | 10 BLISTER PACK in 1 BAG (55154-8148-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2015-06-10 | 0000-00-00 | No | No | Current |