NDC 66336-059 Acetaminophen And Codeine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66336 - Dispensing Solutions, Inc.
- 66336-059 - Acetaminophen And Codeine
Product Characteristics
Product Packages
NDC Code 66336-059-06
Package Description: 6 TABLET in 1 BOTTLE
NDC Code 66336-059-10
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 66336-059-12
Package Description: 12 TABLET in 1 BOTTLE
NDC Code 66336-059-15
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 66336-059-16
Package Description: 16 TABLET in 1 BOTTLE
NDC Code 66336-059-20
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 66336-059-24
Package Description: 24 TABLET in 1 BOTTLE
NDC Code 66336-059-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 66336-059-40
Package Description: 40 TABLET in 1 BOTTLE
NDC Code 66336-059-60
Package Description: 60 TABLET in 1 BOTTLE
Product Details
What is NDC 66336-059?
What are the uses for Acetaminophen And Codeine?
Which are Acetaminophen And Codeine UNII Codes?
The UNII codes for the active ingredients in this product are:
- CODEINE PHOSPHATE (UNII: GSL05Y1MN6)
- CODEINE (UNII: Q830PW7520) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Acetaminophen And Codeine 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:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Acetaminophen And Codeine?
- RxCUI: 993781 - codeine phosphate 30 MG / acetaminophen 300 MG Oral Tablet
- RxCUI: 993781 - acetaminophen 300 MG / codeine phosphate 30 MG Oral Tablet
- RxCUI: 993781 - APAP 300 MG / codeine phosphate 30 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".