73764-001 NDC - ISOPROPYL ALCOHOL ()

Drug Information

Product NDC: 73764-001

Proprietary Name: Isopropyl Alcohol

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Marine Essence Biosciences Corporation of USA
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/23/2020

Package Information

No. Package Code Package Description Billing Unit
173764-001-01500 mL in 1 BOTTLE, PUMP (73764-001-01)
273764-001-02236 mL in 1 BOTTLE, PUMP (73764-001-02)
373764-001-03177 mL in 1 BOTTLE, PUMP (73764-001-03)
473764-001-04473 mL in 1 BOTTLE, PUMP (73764-001-04)
573764-001-05250 mL in 1 BOTTLE, PUMP (73764-001-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73764-001The 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 NAMEIsopropyl AlcoholThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/23/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMarine Essence Biosciences Corporation of USAName 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