NDC 11822-3313 Nicotine Polacrilex

Product Information

What is NDC 11822-3313?

The NDC code 11822-3313 is assigned by the FDA to the product Nicotine Polacrilex which is product labeled by Rite Aid Corporation. The product's dosage form is and is administered via form. The product is distributed in 3 packages with assigned NDC codes 11822-3313-6 100 blister pack in 1 carton / 1 gum, chewing in 1 blister pack, 11822-3313-8 160 blister pack in 1 carton / 1 gum, chewing in 1 blister pack, 11822-3313-9 20 blister pack in 1 carton / 1 gum, chewing in 1 blister pack. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code11822-3313
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Nicotine Polacrilex
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Rite Aid Corporation
Labeler Code11822
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
01-31-2020
Listing Expiration Date What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
12-31-2022
Exclude Flag What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
I
NDC Code Structure

What are the uses for Nicotine Polacrilex?


Product Characteristics

Color(s)WHITE (C48325)
ShapeSQUARE (C48350)
Size(s)14 MM
Score1
Flavor(s)MINT (C73404 - ICE)

Product Packages

NDC Code 11822-3313-6

Package Description: 100 BLISTER PACK in 1 CARTON / 1 GUM, CHEWING in 1 BLISTER PACK

NDC Code 11822-3313-8

Package Description: 160 BLISTER PACK in 1 CARTON / 1 GUM, CHEWING in 1 BLISTER PACK

NDC Code 11822-3313-9

Package Description: 20 BLISTER PACK in 1 CARTON / 1 GUM, CHEWING in 1 BLISTER PACK

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Nicotine Polacrilex Active Ingredients UNII Codes

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

Nicotine Polacrilex Inactive Ingredients UNII Codes

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

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Nicotine Polacrilex Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



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