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  4. NDC Product Code: 16590-556 Pentazocine Hcl And Naloxone Hcl

NDC 16590-556 Pentazocine Hcl And Naloxone Hcl

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 16590-556?
  5. Pentazocine Hcl And Naloxone Hcl 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:
16590-556
Proprietary Name:
Pentazocine Hcl And Naloxone Hcl
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Stat Rx Usa Llc
Labeler Code:
16590
Product Label ID:
1e2de757-cfe1-4731-93d1-36f80175ef33
Start Marketing Date: [9]
01-21-1997
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329 - LIGHT GREEN)
Shape:
OVAL (C48345)
Size(s):
2 MM
Imprint(s):
WATSON;395;50;05
Score:
2

Code Structure Chart

Product Details

What is NDC 16590-556?

The NDC code 16590-556 is assigned by the FDA to the product Pentazocine Hcl And Naloxone Hcl which is product labeled by Stat Rx Usa Llc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 16590-556-30 30 tablet in 1 bottle , 16590-556-40 40 tablet in 1 bottle , 16590-556-60 60 tablet in 1 bottle , 16590-556-72 120 tablet in 1 bottle , 16590-556-90 90 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 Hcl And Naloxone Hcl?

INDICATIONS AND USAGEPentazocine and naloxone hydrochlorides tablets are intended for oral use only. Severe, potentially lethal, reactions may result from misuse of pentazocine and naloxone hydrochlorides tablets by injection either alone or in combination with other substances. (See DRUG ABUSE AND DEPENDENCE section.)Pentazocine and naloxone hydrochlorides tablets are indicated for the relief of moderate to severe pain.Pentazocine and naloxone hydrochlorides tablets are indicated for oral use only.

Which are Pentazocine Hcl And Naloxone Hcl UNII Codes?

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

Which are Pentazocine Hcl And Naloxone Hcl 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 Hcl And Naloxone Hcl?

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: 312289 - pentazocine 50 MG / naloxone 0.5 MG Oral Tablet
  • RxCUI: 312289 - naloxone 0.5 MG / pentazocine 50 MG Oral Tablet
  • RxCUI: 312289 - naloxone (as naloxone hydrochloride) 0.5 MG / pentazocine (as pentazocine hydrochloride) 50 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".