NDC 70199-032

Zyloprim

Allopurinol

Zyloprim is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Casper Pharma Llc. The primary component is Allopurinol.

• Product ID: 70199-032_a78bda09-7bbe-413b-b192-b0b76e0194f7
• NDC: 70199-032
• Product Type: Human Prescription Drug
• Proprietary Name: Zyloprim
• Generic Name: Allopurinol
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2022-08-04
• Marketing Category: NDA /
• Application Number: NDA016084
• Labeler Name: Casper Pharma LLC
• Substance Name: ALLOPURINOL
• Active Ingredient Strength: 200 mg/1
• Pharm Classes: Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 70199-032-01

100 TABLET in 1 BOTTLE (70199-032-01)

• Marketing Start Date: 2022-08-04
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

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

NDC	Brand Name	Generic Name
70199-016	Zyloprim	Zyloprim
70199-015	Zyloprim	Zyloprim
70518-0551	ZYLOPRIM	ZYLOPRIM
65483-991	ZYLOPRIM	ZYLOPRIM
65483-993	ZYLOPRIM	ZYLOPRIM
67046-681	Zyloprim	Zyloprim
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