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U.S. Department of Health and Human Services

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Search results from the "OB_Rx" table for query on "020164."



Active Ingredient: ENOXAPARIN SODIUM
Dosage Form;Route: INJECTABLE;SUBCUTANEOUS
Proprietary Name: LOVENOX (PRESERVATIVE FREE)
Applicant: SANOFI AVENTIS US
Strength: 30MG/0.3ML (100MG/ML)
Application Number: N020164
Product Number: 001
Approval Date: Mar 29, 1993
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AP
Patent and Exclusivity Info for this product: View

Active Ingredient: ENOXAPARIN SODIUM
Dosage Form;Route: INJECTABLE;SUBCUTANEOUS
Proprietary Name: LOVENOX (PRESERVATIVE FREE)
Applicant: SANOFI AVENTIS US
Strength: 40MG/0.4ML (100MG/ML)
Application Number: N020164
Product Number: 002
Approval Date: Jan 30, 1998
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AP
Patent and Exclusivity Info for this product: View

Active Ingredient: ENOXAPARIN SODIUM
Dosage Form;Route: INJECTABLE;SUBCUTANEOUS
Proprietary Name: LOVENOX (PRESERVATIVE FREE)
Applicant: SANOFI AVENTIS US
Strength: 60MG/0.6ML (100MG/ML)
Application Number: N020164
Product Number: 003
Approval Date: Mar 27, 1998
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AP
Patent and Exclusivity Info for this product: View

Active Ingredient: ENOXAPARIN SODIUM
Dosage Form;Route: INJECTABLE;SUBCUTANEOUS
Proprietary Name: LOVENOX (PRESERVATIVE FREE)
Applicant: SANOFI AVENTIS US
Strength: 80MG/0.8ML (100MG/ML)
Application Number: N020164
Product Number: 004
Approval Date: Mar 27, 1998
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AP
Patent and Exclusivity Info for this product: View

Active Ingredient: ENOXAPARIN SODIUM
Dosage Form;Route: INJECTABLE;SUBCUTANEOUS
Proprietary Name: LOVENOX (PRESERVATIVE FREE)
Applicant: SANOFI AVENTIS US
Strength: 100MG/ML (100MG/ML)
Application Number: N020164
Product Number: 005
Approval Date: Mar 27, 1998
Reference Listed Drug Yes
RX/OTC/DISCN: RX
TE Code: AP
Patent and Exclusivity Info for this product: View

Active Ingredient: ENOXAPARIN SODIUM
Dosage Form;Route: INJECTABLE;SUBCUTANEOUS
Proprietary Name: LOVENOX (PRESERVATIVE FREE)
Applicant: SANOFI AVENTIS US
Strength: 120MG/0.8ML (150MG/ML)
Application Number: N020164
Product Number: 007
Approval Date: Jun 2, 2000
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AP
Patent and Exclusivity Info for this product: View

Active Ingredient: ENOXAPARIN SODIUM
Dosage Form;Route: INJECTABLE;SUBCUTANEOUS
Proprietary Name: LOVENOX (PRESERVATIVE FREE)
Applicant: SANOFI AVENTIS US
Strength: 150MG/ML (150MG/ML)
Application Number: N020164
Product Number: 008
Approval Date: Jun 2, 2000
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AP
Patent and Exclusivity Info for this product: View

Active Ingredient: ENOXAPARIN SODIUM
Dosage Form;Route: INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Proprietary Name: LOVENOX
Applicant: SANOFI AVENTIS US
Strength: 300MG/3ML (100MG/ML)
Application Number: N020164
Product Number: 009
Approval Date: Jan 23, 2003
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

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FDA/Center for Drug Evaluation and Research
Office of Generic Drugs
Division of Labeling and Program Support
Update Frequency:

Orange Book Data - Monthly
Generic Drug Product Information & Patent Information - Daily
Orange Book Data Updated Through July 2014
Patent and Generic Drug Product Data Last Updated August 29, 2014

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