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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 017433

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PRE-OP (HEXACHLOROPHENE)
480MG
Marketing Status: Prescription
Active Ingredient: HEXACHLOROPHENE
Proprietary Name: PRE-OP
Dosage Form; Route of Administration: SPONGE; TOPICAL
Strength: 480MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AT
Application Number: N017433
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: DAVIS AND GECK DIV AMERICAN CYANAMID CO
Marketing Status:  Prescription
Patent and Exclusivity Information
PRE-OP II (HEXACHLOROPHENE)
480MG
Marketing Status: Prescription
Active Ingredient: HEXACHLOROPHENE
Proprietary Name: PRE-OP II
Dosage Form; Route of Administration: SPONGE; TOPICAL
Strength: 480MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AT
Application Number: N017433
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: DAVIS AND GECK DIV AMERICAN CYANAMID CO
Marketing Status:  Prescription
Patent and Exclusivity Information
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