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  4. NDC Product Code: 70934-599 Pluspharma Extra Strength Pain Reliever,fever Reducer 500 Mg

NDC 70934-599 Pluspharma Extra Strength Pain Reliever,fever Reducer 500 Mg

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 70934-599?
  5. Pluspharma Extra Strength Pain Reliever,fever Reducer 500 Mg Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
70934-599
Proprietary Name:
Pluspharma Extra Strength Pain Reliever,fever Reducer 500 Mg
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Denton Pharma, Inc. Dba Northwind Pharmaceuticals
Labeler Code:
70934
Product Label ID:
ab94d47d-b2da-5b6a-e053-2995a90a7a84
Start Marketing Date: [9]
03-04-2020
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
Imprint(s):
GPI;A5
Score:
2

Product Packages

NDC Code 70934-599-30

Package Description: 30 TABLET in 1 BOTTLE, PLASTIC

NDC Code 70934-599-90

Package Description: 90 TABLET in 1 BOTTLE, PLASTIC

Product Details

What is NDC 70934-599?

The NDC code 70934-599 is assigned by the FDA to the product Pluspharma Extra Strength Pain Reliever,fever Reducer 500 Mg which is product labeled by Denton Pharma, Inc. Dba Northwind Pharmaceuticals. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 70934-599-30 30 tablet in 1 bottle, plastic , 70934-599-90 90 tablet 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 and RxNorm crosswalk.

What are the uses for Pluspharma Extra Strength Pain Reliever,fever Reducer 500 Mg?

Do not take more than directed (see overdose warning) Adults and children 12 years and over:take 2 tablets every 6 hours while symptoms lastdo not take more than 6 tablets in 24 hours unless directed by a doctordo not take for more than 10 days unless directed by a doctor.Children under 12 years: ask a doctor.

Which are Pluspharma Extra Strength Pain Reliever,fever Reducer 500 Mg UNII Codes?

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

Which are Pluspharma Extra Strength Pain Reliever,fever Reducer 500 Mg 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 Pluspharma Extra Strength Pain Reliever,fever Reducer 500 Mg?

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 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".