Ciprofloxacin
- Product NDC
- 68084-069
- 11-digit product format
- 680840069
- Labeler code
- 68084
- Product ID
- 68084-069_c5979601-eae3-6dc7-e053-2995a90a3118
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA076794
- Marketing category
- ANDA
- Marketing start
- 2004-08-18
- Marketing end
- 2021-10-31
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 68084-069-01 | 68084006901 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-069-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-069-11) | 100 blister pack | 2004-08-18 | 2021-10-31 | No | No | Current |