70875-500 NDC - SP PHARMA ()

Drug Information

Product NDC: 70875-500

Proprietary Name: SP Pharma

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Simpor Pharma Sdn Bhd
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/1/2016

Package Information

No. Package Code Package Description Billing Unit
170875-500-02200 PACKAGE in 1 BOTTLE (70875-500-02) / 500 mg in 1 PACKAGE (70875-500-01)
270875-500-0420 DOSE PACK in 1 CARTON (70875-500-04) / 1500 mg in 1 DOSE PACK (70875-500-03)
370875-500-0530 DOSE PACK in 1 CARTON (70875-500-05) / 1500 mg in 1 DOSE PACK (70875-500-03)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70875-500The 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 NAMESP PharmaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/1/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESimpor Pharma Sdn BhdName 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