NDC 0143-9581 Sertraline Hydrochloride

Product Information

NDC Product Code0143-9581
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.
Sertraline Hydrochloride
NDC Directory StatusINACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
West-ward Pharmaceutical Corp
Labeler Code0143
SPL SET ID:0aee46a9-7c7e-4363-a05d-bf2595930f03
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.
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.
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".
NDC Code Structure

Product Characteristics

Color(s)GREEN (C48329 - LIGHT GREEN)
ShapeOVAL (C48345)
Size(s)10 MM
12 MM

Product Packages

NDC Code 0143-9581-05

Package Description: 500 TABLET, FILM COATED in 1 BOTTLE

Price per Unit: $0.05140 per EA

NDC Code 0143-9581-09

Package Description: 90 TABLET, FILM COATED in 1 BOTTLE

Price per Unit: $0.05140 per EA

NDC Code 0143-9581-30

Package Description: 30 TABLET, FILM COATED in 1 BOTTLE

Price per Unit: $0.05140 per EA

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

Product Details

What is NDC 0143-9581?

The NDC code 0143-9581 is assigned by the FDA to the product Sertraline Hydrochloride which is product labeled by West-ward Pharmaceutical Corp. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 0143-9581-05 500 tablet, film coated in 1 bottle , 0143-9581-09 90 tablet, film coated in 1 bottle , 0143-9581-30 30 tablet, film coated in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sertraline Hydrochloride?

All Dosage Forms of Sertraline Hydrochloride:Concomitant use in patients taking monoamine oxidase inhibitors (MAOIs) is contraindicated (see WARNINGS). Concomitant use in patients taking pimozide is contraindicated (see PRECAUTIONS). Sertraline hydrochloride is contraindicated in patients with a hypersensitivity to sertraline or any of the inactive ingredients in sertraline hydrochloride tablets.

Which are Sertraline Hydrochloride UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Sertraline Hydrochloride 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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Sertraline Hydrochloride?

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:

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Product Label

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