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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 207350

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MAGNESIUM SULFATE IN PLASTIC CONTAINER (MAGNESIUM SULFATE)
2GM/50ML (40MG/ML)
Marketing Status: Prescription
Active Ingredient: MAGNESIUM SULFATE
Proprietary Name: MAGNESIUM SULFATE IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 2GM/50ML (40MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A207350
Product Number: 001
Approval Date: Dec 6, 2017
Applicant Holder Full Name: HQ SPECIALTY PHARMA CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
MAGNESIUM SULFATE IN PLASTIC CONTAINER (MAGNESIUM SULFATE)
4GM/100ML (40MG/ML)
Marketing Status: Prescription
Active Ingredient: MAGNESIUM SULFATE
Proprietary Name: MAGNESIUM SULFATE IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 4GM/100ML (40MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A207350
Product Number: 002
Approval Date: Dec 6, 2017
Applicant Holder Full Name: HQ SPECIALTY PHARMA CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
MAGNESIUM SULFATE IN PLASTIC CONTAINER (MAGNESIUM SULFATE)
4GM/50ML (80MG/ML)
Marketing Status: Prescription
Active Ingredient: MAGNESIUM SULFATE
Proprietary Name: MAGNESIUM SULFATE IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 4GM/50ML (80MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A207350
Product Number: 003
Approval Date: Dec 6, 2017
Applicant Holder Full Name: HQ SPECIALTY PHARMA CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
MAGNESIUM SULFATE IN PLASTIC CONTAINER (MAGNESIUM SULFATE)
20GM/500ML (40MG/ML)
Marketing Status: Prescription
Active Ingredient: MAGNESIUM SULFATE
Proprietary Name: MAGNESIUM SULFATE IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20GM/500ML (40MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A207350
Product Number: 004
Approval Date: Dec 6, 2017
Applicant Holder Full Name: HQ SPECIALTY PHARMA CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
MAGNESIUM SULFATE IN PLASTIC CONTAINER (MAGNESIUM SULFATE)
40GM/1000ML (40MG/ML)
Marketing Status: Prescription
Active Ingredient: MAGNESIUM SULFATE
Proprietary Name: MAGNESIUM SULFATE IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 40GM/1000ML (40MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A207350
Product Number: 005
Approval Date: Dec 6, 2017
Applicant Holder Full Name: HQ SPECIALTY PHARMA CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
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