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  4. NDC Product Code: 50332-0116 Backprin

NDC 50332-0116 Backprin

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50332-0116?
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50332-0116
Proprietary Name:
Backprin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hart Health
Labeler Code:
50332
Product Label ID:
a9301898-2c72-4ec0-bba1-1a2eb1962a38
Start Marketing Date: [9]
07-14-2000
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
12 MM
Score:
1

Product Packages

NDC Code 50332-0116-2

Package Description: 125 PACKET in 1 BOX, UNIT-DOSE / 2 TABLET in 1 PACKET

NDC Code 50332-0116-4

Package Description: 50 PACKET in 1 BOX, UNIT-DOSE / 2 TABLET in 1 PACKET

Product Details

What is NDC 50332-0116?

The NDC code 50332-0116 is assigned by the FDA to the product Backprin which is product labeled by Hart Health. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 50332-0116-2 125 packet in 1 box, unit-dose / 2 tablet in 1 packet, 50332-0116-4 50 packet in 1 box, unit-dose / 2 tablet in 1 packet. 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.

Which are Backprin UNII Codes?

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

Which are Backprin 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 Backprin?

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: 283274 - acetaminophen 250 MG / caffeine 50 MG / magnesium salicylate 290 MG Oral Tablet
  • RxCUI: 283274 - APAP 250 MG / Caffeine 50 MG / Magnesium Salicylate 290 MG Oral Tablet
  • RxCUI: 884770 - BACKPRIN 250 MG / 50 MG / 290 MG Oral Tablet
  • RxCUI: 884770 - acetaminophen 250 MG / caffeine 50 MG / magnesium salicylate 290 MG Oral Tablet [Backprin]
  • RxCUI: 884770 - APAP 250 MG / Caffeine 50 MG / Magnesium Salicylate 290 MG Oral Tablet [Backprin]

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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] 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".