NDC 43386-670 Pentazocine Hydrochloride And Acetaminophen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43386 - Gavis Pharmaceuticals, Llc
- 43386-670 - Pentazocine Hydrochloride And Acetaminophen
Product Characteristics
Product Packages
Product Details
What is NDC 43386-670?
What are the uses for Pentazocine Hydrochloride And Acetaminophen?
Which are Pentazocine Hydrochloride And Acetaminophen UNII Codes?
The UNII codes for the active ingredients in this product are:
- PENTAZOCINE HYDROCHLORIDE (UNII: A36BXO4PPX)
- PENTAZOCINE (UNII: RP4A60D26L) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Pentazocine Hydrochloride And 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Pentazocine Hydrochloride And Acetaminophen?
- RxCUI: 312288 - pentazocine 25 MG / acetaminophen 650 MG Oral Tablet
- RxCUI: 312288 - acetaminophen 650 MG / pentazocine 25 MG Oral Tablet
- RxCUI: 312288 - APAP 650 MG / pentazocine (as pentazocine hydrochloride) 25 MG Oral Tablet
- RxCUI: 312288 - APAP 650 MG / Pentazocine 25 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".