NDC 67457-978

Aloprim

Allopurinol

Aloprim is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Mylan Institutional Llc. The primary component is Allopurinol.

• Product ID: 67457-978_018525b1-e37d-4ff2-9dc3-36b3d90ac3e0
• NDC: 67457-978
• Product Type: Human Prescription Drug
• Proprietary Name: Aloprim
• Generic Name: Allopurinol
• Dosage Form: Injection, Powder, Lyophilized, For Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2020-11-18
• Marketing Category: NDA / NDA
• Application Number: NDA020298
• Labeler Name: Mylan Institutional LLC
• Substance Name: ALLOPURINOL
• Active Ingredient Strength: 500 mg/25mL
• Pharm Classes: Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 67457-978-50

1 VIAL, GLASS in 1 CARTON (67457-978-50) > 25 mL in 1 VIAL, GLASS

• Marketing Start Date: 2020-11-18
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Aloprim" or generic name "Allopurinol"

NDC	Brand Name	Generic Name
67457-187	Aloprim	Aloprim
67457-978	Aloprim	Aloprim
0378-0137	Allopurinol	allopurinol
0378-0181	Allopurinol	allopurinol
0591-5543	Allopurinol	Allopurinol
0591-5544	Allopurinol	Allopurinol
0603-2115	Allopurinol	allopurinol
0603-2116	Allopurinol	allopurinol
0615-1592	Allopurinol	Allopurinol
0615-1593	Allopurinol	Allopurinol
0615-8321	Allopurinol	Allopurinol
0615-8385	Allopurinol	allopurinol
0904-6571	Allopurinol	allopurinol
0904-6572	Allopurinol	allopurinol
0904-7041	Allopurinol	Allopurinol
10544-545	Allopurinol	Allopurinol
10544-547	Allopurinol	Allopurinol
10544-911	Allopurinol	Allopurinol
16571-883	Allopurinol	allopurinol
16571-884	Allopurinol	allopurinol
16571-885	Allopurinol	allopurinol
16714-041	Allopurinol	Allopurinol
16714-042	Allopurinol	Allopurinol