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  4. NDC Product Code: 16103-389 Pharbinex-pe

NDC 16103-389 Pharbinex-pe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 16103-389?
  5. Pharbinex-pe 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:
16103-389
Proprietary Name:
Pharbinex-pe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pharbest Pharmaceuticals, Inc.
Labeler Code:
16103
Product Label ID:
cad73d08-a439-446f-aaa9-d1fd18ec1e54
Start Marketing Date: [9]
05-01-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
CAPSULE (C48336)
Size(s):
19 MM
Imprint(s):
PH043
Score:
2

Product Packages

NDC Code 16103-389-04

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 30 TABLET, COATED in 1 BOTTLE, PLASTIC

Product Details

What is NDC 16103-389?

The NDC code 16103-389 is assigned by the FDA to the product Pharbinex-pe which is product labeled by Pharbest Pharmaceuticals, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 16103-389-04 1 bottle, plastic in 1 carton / 30 tablet, coated in 1 bottle, plastic. 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 Pharbinex-pe?

Take with a full glass of waterthis product can be administered without regard for the timing of mealsdo not exceed 6 doses in 24 hours or as directed by doctoradults and children 12 years of age and overtake 1 caplet every 4 hours as neededchildren 6 to under 12 years of agetake ½ caplet every 4 hours as neededchildren under 6 years of ageconsult a doctor

Which are Pharbinex-pe UNII Codes?

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

Which are Pharbinex-pe 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 Pharbinex-pe?

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: 1304111 - guaiFENesin 400 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1304111 - guaifenesin 400 MG / phenylephrine hydrochloride 10 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".