71309-113 NDC - SENNA-DOC ()

Drug Information

Product NDC: 71309-113

Proprietary Name: Senna-Doc

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: 3014704014
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/7/2016

Package Information

No. Package Code Package Description Billing Unit
171309-113-022 POUCH in 1 POUCH (71309-113-02) / 2 TABLET, COATED in 1 POUCH
271309-113-101000 BOTTLE in 1 BOTTLE (71309-113-10) / 500 BOTTLE in 1 BOTTLE (71309-113-05) / 24 CARTON in 1 BOTTLE (71309-113-24) / 1 TABLET, COATED in 1 CARTON
371309-113-2525 POUCH in 1 BOX (71309-113-25) / 2 TABLET, COATED in 1 POUCH
471309-113-5050 POUCH in 1 BOX (71309-113-50) / 2 TABLET, COATED in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC71309-113The 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 NAMESenna-DocThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/7/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME3014704014Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023