NDC 43386-670 Pentazocine Hydrochloride And Acetaminophen

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
43386-670
Proprietary Name:
Pentazocine Hydrochloride And Acetaminophen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gavis Pharmaceuticals, Llc
Labeler Code:
43386
Start Marketing Date: [9]
05-11-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
CAPSULE (C48336)
Size(s):
19 MM
Imprint(s):
NL;670
Score:
2

Product Packages

NDC Code 43386-670-01

Package Description: 100 TABLET in 1 BOTTLE

Price per Unit: $0.87773 per EA

Product Details

What is NDC 43386-670?

The NDC code 43386-670 is assigned by the FDA to the product Pentazocine Hydrochloride And Acetaminophen which is product labeled by Gavis Pharmaceuticals, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43386-670-01 100 tablet in 1 bottle . 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 Pentazocine Hydrochloride And Acetaminophen?

Pentazocine Hydrochloride and Acetaminophen Tablets are indicated for the relief of mild to moderate pain.

Which are Pentazocine Hydrochloride And Acetaminophen UNII Codes?

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

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:

What is the NDC to RxNorm Crosswalk for Pentazocine Hydrochloride And Acetaminophen?

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: 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

* 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".