70735-070 NDC - ASPICARE ()

Drug Information

Product NDC: 70735-070

Proprietary Name: AspiCare

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: American Private Label Products
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/9/2020

Package Information

No. Package Code Package Description Billing Unit
170735-070-0130 mL in 1 BOTTLE (70735-070-01)
270735-070-0260 mL in 1 BOTTLE (70735-070-02)
370735-070-0389 mL in 1 BOTTLE (70735-070-03)
470735-070-04118 mL in 1 BOTTLE (70735-070-04)
570735-070-06177 mL in 1 BOTTLE (70735-070-06)
670735-070-08236 mL in 1 BOTTLE (70735-070-08)
770735-070-16473 mL in 1 BOTTLE (70735-070-16)
870735-070-32946 mL in 1 BOTTLE (70735-070-32)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70735-070The 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 NAMEAspiCareThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/9/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAmerican Private Label ProductsName 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