68682-012 NDC - ETHACRYNIC SODIUM ()

Drug Information

Product NDC: 68682-012

Proprietary Name: ethacrynic sodium

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Pharmacy Class(es):

No.	Package Code	Package Description	Billing Unit
1	68682-012-27	1 VIAL in 1 CARTON (68682-012-27) / 50 mL in 1 VIAL	EA
2	68682-012-50	1 VIAL in 1 CARTON (68682-012-50) / 50 mL in 1 VIAL	EA

Field Name	Field Value	Definition
PRODUCT NDC	68682-012	The 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 NAME	ethacrynic sodium	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	1/10/1967	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Oceanside Pharmaceuticals	Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC	68682-012	The 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 NAME	ethacrynic sodium	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	1/10/1967	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Oceanside Pharmaceuticals	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