NDC 33261-840 Nifedipine

Product Information

What is NDC 33261-840?

The NDC code 33261-840 is assigned by the FDA to the product Nifedipine which is product labeled by Aidarex Pharmaceuticals Llc. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 33261-840-30 30 tablet, film coated, extended release in 1 bottle, plastic . 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 Code33261-840
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.
Nifedipine
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Aidarex Pharmaceuticals Llc
Labeler Code33261
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.
10-03-2007
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.
12-31-2019
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 Nifedipine?


Product Characteristics

Color(s)PINK (C48328)
ShapeROUND (C48348)
Size(s)12 MM
Imprint(s)KU;262
Score1

Product Packages

NDC Code 33261-840-30

Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

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

Product Details

Nifedipine 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:
  • RxCUI: 1812015 - NIFEdipine 90 MG Osmotic 24HR Extended Release Oral Tablet
  • RxCUI: 1812015 - Osmotic 24 HR nifedipine 90 MG Extended Release Oral Tablet
  • RxCUI: 1812015 - nifedipine 90 MG Osmotic 24 HR Extended Release Oral Tablet

Nifedipine 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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Patient Education

Nifedipine

Nifedipine is pronounced as (nye fed' i peen)

Why is nifedipine medication prescribed?
Nifedipine is used to treat high blood pressure and to control angina (chest pain). Nifedipine is in a class of medications called calcium-channel blockers. It lowers blo...
[Read More]

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Nifedipine 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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