31382-963 NDC - CAREPURE ()

Drug Information

Product NDC: 31382-963

Proprietary Name: CarePure

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Carestream Health, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
131382-963-01208198 mL in 1 DRUM (31382-963-01)
231382-963-0260 mL in 1 BOTTLE (31382-963-02)
331382-963-0380 mL in 1 BOTTLE (31382-963-03)
431382-963-04120 mL in 1 BOTTLE (31382-963-04)
531382-963-05240 mL in 1 BOTTLE (31382-963-05)
631382-963-06500 mL in 1 BOTTLE (31382-963-06)
731382-963-071000 mL in 1 CONTAINER (31382-963-07)
831382-963-084000 mL in 1 CONTAINER (31382-963-08)
931382-963-095000 mL in 1 CONTAINER (31382-963-09)
1031382-963-1010000 mL in 1 CONTAINER (31382-963-10)
1131382-963-117571 mL in 1 CONTAINER (31382-963-11)
1231382-963-1218927 mL in 1 CONTAINER (31382-963-12)
1331382-963-13250 mL in 1 BOTTLE (31382-963-13)

NDC Record

Field Name Field Value Definition
PRODUCT NDC31382-963The 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 NAMECarePureThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX01A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE3/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECarestream Health, Inc.Name 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