78036-001 NDC - CHEMBRITE ()

Drug Information

Product NDC: 78036-001

Proprietary Name: ChemBrite

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Interion Pte Ltd
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/25/2020

Package Information

No. Package Code Package Description Billing Unit
178036-001-01200 mL in 1 BOTTLE (78036-001-01)
278036-001-02250 mL in 1 BOTTLE (78036-001-02)
378036-001-03500 mL in 1 BOTTLE (78036-001-03)
478036-001-041000 mL in 1 BOTTLE (78036-001-04)
578036-001-055000 mL in 1 CONTAINER (78036-001-05)
678036-001-0610000 mL in 1 CONTAINER (78036-001-06)
778036-001-0720000 mL in 1 CONTAINER (78036-001-07)
878036-001-0825000 mL in 1 CONTAINER (78036-001-08)
978036-001-0930000 mL in 1 CONTAINER (78036-001-09)
1078036-001-10200000 mL in 1 CONTAINER (78036-001-10)
1178036-001-11209000 mL in 1 CONTAINER (78036-001-11)
1278036-001-121000000 mL in 1 CONTAINER (78036-001-12)

NDC Record

Field Name Field Value Definition
PRODUCT NDC78036-001The 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 NAMEChemBriteThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/25/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEInterion Pte LtdName 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