12745-105 NDC - ISOPROPYL ALCOHOL ()

Drug Information

Product NDC: 12745-105

Proprietary Name: Isopropyl Alcohol

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Medical Chemical Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/15/1954

Package Information

No. Package Code Package Description Billing Unit
112745-105-01946 mL in 1 BOTTLE, PLASTIC (12745-105-01)
212745-105-033785 mL in 1 BOTTLE, PLASTIC (12745-105-03)
312745-105-043785 mL in 1 BOTTLE, PLASTIC (12745-105-04)
412745-105-0518927 mL in 1 CONTAINER (12745-105-05)
512745-105-0618927 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (12745-105-06)
612745-105-07208198 mL in 1 DRUM (12745-105-07)
712745-105-08473 mL in 1 BOTTLE, PLASTIC (12745-105-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC12745-105The 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 DATE6/15/1954This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMedical Chemical CorporationName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 4/12/2024