Ciloxan
- Product NDC
- 70518-1234
- 11-digit product format
- 705181234
- Labeler code
- 70518
- Product ID
- 70518-1234_d9190c5b-63ca-771b-e053-2995a90a4722
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciprofloxacin hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- REMEDYREPACK INC.
- Application
- NDA019992
- Marketing category
- NDA
- Marketing start
- 2018-05-30
- 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 |
|---|
| 70518-1234-0 | 70518123400 | 1 BOTTLE, PLASTIC in 1 CARTON (70518-1234-0) > 5 mL in 1 BOTTLE, PLASTIC | 2018-05-30 | 0000-00-00 | No | No | Current |