NDC 65437-040 Acetaminophen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65437 - Himprit Pharmachem Pvt Ltd
- 65437-040 - Acetaminophen
Product Characteristics
Product Packages
NDC Code 65437-040-31
Package Description: 1 BAG in 1 DRUM / 31000 TABLET, FILM COATED in 1 BAG
NDC Code 65437-040-50
Package Description: 1 BAG in 1 DRUM / 50000 TABLET, FILM COATED in 1 BAG
Product Details
What is NDC 65437-040?
What are the uses for Acetaminophen?
Which are Acetaminophen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Acetaminophen 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:
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Acetaminophen?
- RxCUI: 198440 - acetaminophen 500 MG Oral Tablet
- RxCUI: 198440 - APAP 500 MG Oral Tablet
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[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".