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  4. NDC Product Code: 68405-037 Hypertenipine

NDC 68405-037 Hypertenipine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68405-037?
  5. Hypertenipine 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:
68405-037
Proprietary Name:
Hypertenipine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Physician Therapeutics Llc
Labeler Code:
68405
Product Label ID:
2fcc87a4-74ef-46bd-8ee9-bd2f3cf3d0c2
Start Marketing Date: [9]
07-07-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape:
ROUND (C48348)
CAPSULE (C48336)
Size(s):
6 MM
21 MM
Imprint(s):
IG;237
;
Score:
1

Code Structure Chart

Product Details

What is NDC 68405-037?

The NDC code 68405-037 is assigned by the FDA to the product Hypertenipine which is product labeled by Physician Therapeutics Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68405-037-36 1 kit in 1 kit * 90 capsule in 1 bottle * 30 tablet in 1 bottle (52959-910-30). 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 Hypertenipine?

INDICATIONS AND USAGE1. HypertensionAmlodipine besylate is indicated for the treatment of hypertension. It may be used alone or incombination with other antihypertensive agents.2. Coronary Artery DiseaseCronic Stable AnginaAmlodipine besylate is indicated for the symptomatic treatment of chronic stable angina.Amlodipine besylate may be used alone or in combination with other antianginal agents.Vasospastic Angina (Prinzmetal’s or Variant Angina)Amlodipine besylate is indicated for the treatment of confirmed or suspected vasospastic angina.Amlodipine besylate may be used as monotherapy or in combination with other antianginal drugs. INDICATIONS FOR USE  Hypertensa is intended for the clinical dietary management of the metabolic processes in patients with hypertension.

Which are Hypertenipine UNII Codes?

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

Which are Hypertenipine 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 Hypertenipine?

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:

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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".