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FDA Approval

Atenolol

CompanyNuCare Pharmaceuticals,Inc. (DUNS: 010632300)

Effective Date

February 17, 2021

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Atenolol(50 mg in 1 1)

Manufacturing Establishments (1)

NuCare Pharmaceuticals,Inc.

Labeler

NuCare Pharmaceuticals,Inc.

DUNS Number

010632300

Products (1)

Atenolol

NDC Product Code

68071-4766

Application Number

ANDA074056

Marketing Category

ANDA (C73584)

Route of Administration

ORAL

Effective Date

February 17, 2021

Ingredients

MAGNESIUM STEARATEInactive

Code: 70097M6I30Class: IACT

POVIDONE K30Inactive

Code: U725QWY32XClass: IACT

SODIUM STARCH GLYCOLATE TYPE A POTATOInactive

Code: 5856J3G2A2Class: IACT

Code: 50VV3VW0TIClass: ACTIBQuantity: 50 mg in 1 1

CELLULOSE, MICROCRYSTALLINEInactive

Code: OP1R32D61UClass: IACT

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