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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 000552

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HEPARIN SODIUM (HEPARIN SODIUM)
1,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: HEPARIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 008
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
HEPARIN SODIUM (HEPARIN SODIUM)
5,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: HEPARIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 009
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
HEPARIN SODIUM (HEPARIN SODIUM)
10,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: HEPARIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 010
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
LIQUAEMIN LOCK FLUSH (HEPARIN SODIUM)
100 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: LIQUAEMIN LOCK FLUSH
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 100 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 007
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
LIQUAEMIN SODIUM (HEPARIN SODIUM)
1,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: LIQUAEMIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
LIQUAEMIN SODIUM (HEPARIN SODIUM)
5,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: LIQUAEMIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
LIQUAEMIN SODIUM (HEPARIN SODIUM)
10,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: LIQUAEMIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
LIQUAEMIN SODIUM (HEPARIN SODIUM)
20,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: LIQUAEMIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
LIQUAEMIN SODIUM (HEPARIN SODIUM)
40,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: LIQUAEMIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 40,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
LIQUAEMIN SODIUM PRESERVATIVE FREE (HEPARIN SODIUM)
1,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: LIQUAEMIN SODIUM PRESERVATIVE FREE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 011
Approval Date: Apr 11, 1986
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
LIQUAEMIN SODIUM PRESERVATIVE FREE (HEPARIN SODIUM)
5,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: LIQUAEMIN SODIUM PRESERVATIVE FREE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 012
Approval Date: Apr 11, 1986
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
LIQUAEMIN SODIUM PRESERVATIVE FREE (HEPARIN SODIUM)
10,000 UNITS/ML
Marketing Status: Discontinued
Active Ingredient: HEPARIN SODIUM
Proprietary Name: LIQUAEMIN SODIUM PRESERVATIVE FREE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N000552
Product Number: 013
Approval Date: Apr 11, 1986
Applicant Holder Full Name: ORGANON USA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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