CIPROFLOXACIN
- Product NDC
- 72189-323
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CIPROFLOXACIN
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA208921
- Marketing category
- ANDA
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72189-323-06 | 6 TABLET, COATED in 1 BOTTLE (72189-323-06) | 2022-02-21 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | Direct Rx | 2025-01-21 | HUMAN PRESCRIPTION DRUG LABEL | 2 |