Ciprofloxacin Hydrochloride
- Product NDC
- 55700-636
- 11-digit product format
- 557000636
- Labeler code
- 55700
- Product ID
- 55700-636_b56a55d9-29fd-497e-b2d9-276a70204f31
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- NDA019992
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2018-06-08
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#