Details for New Drug Application (NDA): 076673
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The generic ingredient in CIPROFLOXACIN HYDROCHLORIDE is ciprofloxacin hydrochloride. There are thirty-four drug master file entries for this compound. Fifty-six suppliers are listed for this compound. Additional details are available on the ciprofloxacin hydrochloride profile page.
Summary for 076673
Tradename: | CIPROFLOXACIN HYDROCHLORIDE |
Applicant: | Watson Labs Inc |
Ingredient: | ciprofloxacin hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 076673
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CIPROFLOXACIN HYDROCHLORIDE | ciprofloxacin hydrochloride | SOLUTION/DROPS;OPHTHALMIC | 076673 | ANDA | Medsource Pharmaceuticals | 45865-772 | 45865-772-01 | 1 BOTTLE, DROPPER in 1 CARTON (45865-772-01) / 10 mL in 1 BOTTLE, DROPPER |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION/DROPS;OPHTHALMIC | Strength | EQ 0.3% BASE | ||||
Approval Date: | Jan 21, 2005 | TE: | AT | RLD: | No |
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