57664-506 NDC - METOPROLOL TARTRATE ()

Drug Information

Product NDC: 57664-506

Proprietary Name: Metoprolol tartrate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Pharmacy Class(es):
  • Adrenergic beta-Antagonists [MoA];
  • beta-Adrenergic Blocker [EPC]

Labeler Information

Labeler Name: Sun Pharmaceutical Industries, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/29/2015

Package Information

No. Package Code Package Description Billing Unit
157664-506-08100 TABLET in 1 BOTTLE (57664-506-08)EA
257664-506-181000 TABLET in 1 BOTTLE (57664-506-18)EA
357664-506-52100 TABLET in 1 BOTTLE (57664-506-52)EA
457664-506-5430 TABLET in 1 BOTTLE (57664-506-54)
557664-506-581000 TABLET in 1 BOTTLE (57664-506-58)EA
657664-506-5990 TABLET in 1 BOTTLE (57664-506-59)
757664-506-8330 TABLET in 1 BOTTLE (57664-506-83)
857664-506-9990 TABLET in 1 BOTTLE (57664-506-99)

NDC Record

Field Name Field Value Definition
PRODUCT NDC57664-506The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEMetoprolol tartrateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/29/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESun Pharmaceutical Industries, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC57664-506The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEMetoprolol tartrateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/29/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESun Pharmaceutical Industries, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023