NDC 70199-033

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 ID70199-033_a78bda09-7bbe-413b-b192-b0b76e0194f7
NDC70199-033
Product TypeHuman Prescription Drug
Proprietary NameZyloprim
Generic NameAllopurinol
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2022-08-04
Marketing CategoryNDA /
Application NumberNDA016084
Labeler NameCasper Pharma LLC
Substance NameALLOPURINOL
Active Ingredient Strength300 mg/1
Pharm ClassesXanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 70199-033-01

100 TABLET in 1 BOTTLE (70199-033-01)
Marketing Start Date2022-08-04
NDC Exclude FlagN
Sample Package?N

Drug Details

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

NDCBrand NameGeneric Name
70199-016ZyloprimZyloprim
70199-015ZyloprimZyloprim
70518-0551ZYLOPRIMZYLOPRIM
65483-991ZYLOPRIMZYLOPRIM
65483-993ZYLOPRIMZYLOPRIM
67046-681ZyloprimZyloprim
0378-0137Allopurinolallopurinol
0378-0181Allopurinolallopurinol
0591-5543AllopurinolAllopurinol
0591-5544AllopurinolAllopurinol
0603-2115Allopurinolallopurinol
0603-2116Allopurinolallopurinol
0615-1592AllopurinolAllopurinol
0615-1593AllopurinolAllopurinol
0615-8321AllopurinolAllopurinol
0615-8385Allopurinolallopurinol
0904-6571Allopurinolallopurinol
0904-6572Allopurinolallopurinol
0904-7041AllopurinolAllopurinol
10544-545AllopurinolAllopurinol
10544-547AllopurinolAllopurinol
10544-911AllopurinolAllopurinol
16571-883Allopurinolallopurinol
16571-884Allopurinolallopurinol
16571-885Allopurinolallopurinol
16714-041AllopurinolAllopurinol
16714-042AllopurinolAllopurinol

Trademark Results [Zyloprim]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ZYLOPRIM
ZYLOPRIM
72180834 0773095 Live/Registered
Burroughs Wellcome & Co. (U.S.A.) Inc.
1963-11-12

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