Ciprofloxacin
- Product NDC
- 55111-128
- 11-digit product format
- 551110128
- Labeler code
- 55111
- Product ID
- 55111-128_ab375e84-e300-962c-6eec-e67f1f9587ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Dr. Reddy's Laboratories Limited
- Application
- ANDA075593
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 750 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55111-128-01 | 55111012801 | 100 TABLET, FILM COATED in 1 BOTTLE (55111-128-01) | | 2004-06-09 | 0000-00-00 | No | No | Current |
| 55111-128-05 | 55111012805 | 500 TABLET, FILM COATED in 1 BOTTLE (55111-128-05) | | 2004-06-09 | 0000-00-00 | No | No | Current |
| 55111-128-50 | 55111012850 | 50 TABLET, FILM COATED in 1 BOTTLE (55111-128-50) | | 2004-06-09 | 0000-00-00 | No | No | Current |
| 55111-128-78 | 55111012878 | 10 DOSE PACK in 1 BOX (55111-128-78) > 10 TABLET, FILM COATED in 1 DOSE PACK (55111-128-79) | 10 dose pack | 2004-06-09 | 0000-00-00 | No | No | Current |