ciprofloxacin
- Product NDC
- 70518-2390
- 11-digit product format
- 705182390
- Labeler code
- 70518
- Product ID
- 70518-2390_e3895d2c-9c6c-993e-e053-2995a90a3a2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077568
- Marketing category
- ANDA
- Marketing start
- 2019-10-25
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2390 | CIPROFLOXACIN SOLUTION [REMEDYREPACK INC.] | 8 | Legacy NDC | 20250316_a0146240-40ae-4b09-9c60-93def8a68cd1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2390-0 | 70518239000 | 1 BOTTLE, PLASTIC in 1 CARTON (70518-2390-0) > 2.5 mL in 1 BOTTLE, PLASTIC | 2019-10-25 | 0000-00-00 | No | No | Current |