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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 210644

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OXYCODONE AND ACETAMINOPHEN (ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE)
325MG;2.5MG
Marketing Status: Prescription
Active Ingredient: ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCODONE AND ACETAMINOPHEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 325MG;2.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A210644
Product Number: 001
Approval Date: Feb 9, 2018
Applicant Holder Full Name: ABHAI LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
OXYCODONE AND ACETAMINOPHEN (ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE)
325MG;5MG
Marketing Status: Prescription
Active Ingredient: ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCODONE AND ACETAMINOPHEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 325MG;5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A210644
Product Number: 002
Approval Date: Feb 9, 2018
Applicant Holder Full Name: ABHAI LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
OXYCODONE AND ACETAMINOPHEN (ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE)
325MG;7.5MG
Marketing Status: Prescription
Active Ingredient: ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCODONE AND ACETAMINOPHEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 325MG;7.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A210644
Product Number: 003
Approval Date: Feb 9, 2018
Applicant Holder Full Name: ABHAI LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
OXYCODONE AND ACETAMINOPHEN (ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE)
325MG;10MG
Marketing Status: Prescription
Active Ingredient: ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Proprietary Name: OXYCODONE AND ACETAMINOPHEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 325MG;10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A210644
Product Number: 004
Approval Date: Feb 9, 2018
Applicant Holder Full Name: ABHAI LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
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