Ciprofloxacin
- Product NDC
- 70518-3417
- 11-digit product format
- 705183417
- Labeler code
- 70518
- Product ID
- 70518-3417_ded1621b-d7f2-6cc7-e053-2995a90a2d42
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2022-05-11
- 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
- 2023-12-31
- 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 |
|---|
| 70518-3417-0 | 70518341700 | 6 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3417-0) | 2022-05-11 | 0000-00-00 | No | No | Current |
| 70518-3417-1 | 70518341701 | 10 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3417-1) | 2022-05-11 | 0000-00-00 | No | No | Current |
| 70518-3417-2 | 70518341702 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3417-2) | 2022-05-11 | 0000-00-00 | No | No | Current |