NDC 68788-2115

Allopurinol

Allopurinol

Allopurinol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is Allopurinol.

• Product ID: 68788-2115_c0ebdd84-8118-44ab-aaf3-135f89b6895f
• NDC: 68788-2115
• Product Type: Human Prescription Drug
• Proprietary Name: Allopurinol
• Generic Name: Allopurinol
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2009-10-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA071586
• Labeler Name: Preferred Pharmaceuticals, Inc.
• Substance Name: ALLOPURINOL
• Active Ingredient Strength: 100 mg/1
• Pharm Classes: Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 68788-2115-9

90 TABLET in 1 BOTTLE (68788-2115-9)

• Marketing Start Date: 2009-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68788-2115-1 [68788211501]

Allopurinol TABLET

• Marketing Category: ANDA
• Application Number: ANDA071586
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-10-01
• Marketing End Date: 2019-05-07

NDC 68788-2115-3 [68788211503]

Allopurinol TABLET

• Marketing Category: ANDA
• Application Number: ANDA071586
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-10-01
• Marketing End Date: 2019-05-07

NDC 68788-2115-9 [68788211509]

Allopurinol TABLET

• Marketing Category: ANDA
• Application Number: ANDA071586
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-10-01
• Marketing End Date: 2019-05-07

Drug Details

Active Ingredients

Ingredient	Strength
ALLOPURINOL	100 mg/1

OpenFDA Data

• SPL SET ID: 3df46df4-8b14-459f-949b-dc1f94a07330
• Manufacturer:
  • Preferred Pharmaceuticals, Inc.
• UNII:
  • 63CZ7GJN5I
• RxNorm Concept Unique ID - RxCUI:
  • 197320
  • 197319

Pharmacological Class

• Xanthine Oxidase Inhibitor [EPC]
• Xanthine Oxidase Inhibitors [MoA]

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

NDC	Brand Name	Generic Name
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
67544-988	Allopurinol	Allopurinol
68071-4131	Allopurinol	Allopurinol
68788-6422	Allopurinol	Allopurinol
68788-2115	Allopurinol	Allopurinol
68788-0603	Allopurinol	Allopurinol
68788-6323	Allopurinol	Allopurinol
68788-7383	Allopurinol	Allopurinol
68788-9331	Allopurinol	Allopurinol
68788-9831	Allopurinol	Allopurinol
68788-9832	Allopurinol	Allopurinol
70518-0429	Allopurinol	Allopurinol
70518-0451	Allopurinol	Allopurinol
70518-0190	Allopurinol	Allopurinol
70518-0476	Allopurinol	Allopurinol
70518-0555	Allopurinol	Allopurinol
70518-1576	Allopurinol	Allopurinol
70518-1678	Allopurinol	Allopurinol
70518-1407	Allopurinol	Allopurinol
70518-1573	Allopurinol	Allopurinol
70710-1209	Allopurinol	Allopurinol
70518-1806	Allopurinol	Allopurinol
70771-1127	Allopurinol	Allopurinol
70710-1210	Allopurinol	Allopurinol
70771-1126	Allopurinol	Allopurinol
71205-049	Allopurinol	Allopurinol
70934-072	Allopurinol	Allopurinol
71335-0599	Allopurinol	Allopurinol
71335-0112	Allopurinol	Allopurinol
71335-0467	Allopurinol	Allopurinol