ciprofloxacin
- Product NDC
- 70518-2045
- 11-digit product format
- 705182045
- Labeler code
- 70518
- Product ID
- 70518-2045_e38935d3-7cda-35dc-e053-2995a90ac751
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077568
- Marketing category
- ANDA
- Marketing start
- 2019-04-29
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 3 mg/mL
- 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 |
|---|
| 70518-2045-0 | 70518204500 | 1 BOTTLE, PLASTIC in 1 CARTON (70518-2045-0) > 2.5 mL in 1 BOTTLE, PLASTIC | 2019-04-29 | 0000-00-00 | No | No | Current |