Ciprofloxacin
- Product NDC
- 0404-7187
- 11-digit product format
- 004047187
- Labeler code
- 0404
- Product ID
- 0404-7187_8dcd3721-e289-4b70-afb7-55215ce6781b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Henry Schein Inc.
- Application
- ANDA076555
- Marketing category
- ANDA
- Marketing start
- 2015-05-13
- 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 |
|---|
| 0404-7187-01 | 00404718701 | 1 BOTTLE, DROPPER in 1 CARTON (0404-7187-01) > 5 mL in 1 BOTTLE, DROPPER | 2015-05-13 | 0000-00-00 | No | No | Current |