69097-535 NDC - PHENYLEPHRINE HYDROCHLORIDE ()

Drug Information

Product NDC: 69097-535

Proprietary Name: Phenylephrine hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Cipla USA Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/1/2018

Package Information

No. Package Code Package Description Billing Unit
169097-535-9610 CARTON in 1 CELLO PACK (69097-535-96) / 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (69097-535-35) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGEML

NDC Record

Field Name Field Value Definition
PRODUCT NDC69097-535The 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 NAMEPhenylephrine 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 DATE6/1/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECipla USA 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