Ciprofloxacin
- Product NDC
- 72789-006
- 11-digit product format
- 727890006
- Labeler code
- 72789
- Product ID
- 72789-006_d22d03ab-7344-6524-e053-2995a90ab66f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA076126
- Marketing category
- ANDA
- Marketing start
- 2009-10-10
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-006-06 | 72789000606 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-006-06) | 2019-09-04 | 0000-00-00 | No | No | Current |