Ciprofloxacin
- Product NDC
- 70518-2202
- 11-digit product format
- 705182202
- Labeler code
- 70518
- Product ID
- 70518-2202_daf8a369-5084-73cf-e053-2995a90ae834
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2019-07-10
- 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
- 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 |
|---|
| 70518-2202-0 | 70518220200 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2202-0) | 2019-07-10 | 0000-00-00 | No | No | Current |
| 70518-2202-1 | 70518220201 | 10 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2202-1) | 2019-07-10 | 0000-00-00 | No | No | Current |
| 70518-2202-2 | 70518220202 | 30 TABLET, COATED in 1 BLISTER PACK (70518-2202-2) | 2019-07-11 | 0000-00-00 | No | No | Current |