68071-3310 NDC - DICYCLOMINE HYDROCHLORIDE ()

Drug Information

Product NDC: 68071-3310

Proprietary Name: Dicyclomine Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: NuCare Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/19/1986

Package Information

No. Package Code Package Description Billing Unit
168071-3310-116 CAPSULE in 1 BOTTLE (68071-3310-1)
268071-3310-330 CAPSULE in 1 BOTTLE (68071-3310-3)
368071-3310-660 CAPSULE in 1 BOTTLE (68071-3310-6)
468071-3310-990 CAPSULE in 1 BOTTLE (68071-3310-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC68071-3310The 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 NAMEDicyclomine HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/19/1986This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENuCare Pharmaceuticals, 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