Ciprofloxacin Hydrochloride
- Product NDC
- 68788-7100
- 11-digit product format
- 687887100
- Labeler code
- 68788
- Product ID
- 68788-7100_ccd565b4-773e-4b62-a6bb-827c432984dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Preferred Preferred Phamraceuticals Inc. Inc.
- Application
- NDA019992
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2018-03-12
- 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
- 2021-12-31
- 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 |
|---|
| 68788-7100-5 | 68788710005 | 1 BOTTLE, PLASTIC in 1 CARTON (68788-7100-5) > 5 mL in 1 BOTTLE, PLASTIC | 2018-03-12 | 0000-00-00 | No | No | Current |