70692-119 NDC - ACETAMINOPHEN 500MG DIPHENHYDRAMINE HCL 25MG ()

Drug Information

Product NDC: 70692-119

Proprietary Name: Acetaminophen 500mg Diphenhydramine HCl 25mg

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Strive Pharmaceuticals Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/20/2018

Package Information

No. Package Code Package Description Billing Unit
170692-119-0550 TABLET in 1 PACKAGE (70692-119-05)
270692-119-414 TABLET in 1 PACKAGE (70692-119-41)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70692-119The 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 NAMEAcetaminophen 500mg Diphenhydramine HCl 25mgThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/20/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEStrive Pharmaceuticals IncName 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