NDC 71335-1083 Lisinopril And Hydrochlorothiazide
Tablet Oral

Product Information

What is NDC 71335-1083?

The NDC code 71335-1083 is assigned by the FDA to the product Lisinopril And Hydrochlorothiazide which is a human prescription drug product labeled by Bryant Ranch Prepack. The product's dosage form is tablet and is administered via oral form. The product is distributed in 6 packages with assigned NDC codes 71335-1083-1 30 tablet in 1 bottle , 71335-1083-2 60 tablet in 1 bottle , 71335-1083-3 90 tablet in 1 bottle , 71335-1083-4 120 tablet in 1 bottle , 71335-1083-5 100 tablet in 1 bottle , 71335-1083-6 180 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, RxNorm crosswalk and the complete product label.

NDC Product Code71335-1083
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Lisinopril And Hydrochlorothiazide
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Lisinopril And Hydrochlorothiazide
Product Type What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Human Prescription Drug
Dosage FormTablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Bryant Ranch Prepack
Labeler Code71335
FDA Application Number What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
ANDA076194
Marketing Category What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
03-04-2003
Listing Expiration Date 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.
12-31-2023
Exclude Flag 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".
N
NDC Code Structure

What are the uses for Lisinopril And Hydrochlorothiazide?


Product Characteristics

Color(s)PINK (C48328)
ShapeROUND (C48348)
Size(s)10 MM
Imprint(s)WATSON;862
Score1

Product Packages

NDC Code 71335-1083-1

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 71335-1083-2

Package Description: 60 TABLET in 1 BOTTLE

NDC Code 71335-1083-3

Package Description: 90 TABLET in 1 BOTTLE

NDC Code 71335-1083-4

Package Description: 120 TABLET in 1 BOTTLE

NDC Code 71335-1083-5

Package Description: 100 TABLET in 1 BOTTLE

NDC Code 71335-1083-6

Package Description: 180 TABLET in 1 BOTTLE

Product Details

What are Lisinopril And Hydrochlorothiazide Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • HYDROCHLOROTHIAZIDE 25 mg/1 - A thiazide diuretic often considered the prototypical member of this class. It reduces the reabsorption of electrolytes from the renal tubules. This results in increased excretion of water and electrolytes, including sodium, potassium, chloride, and magnesium. It is used in the treatment of several disorders including edema, hypertension, diabetes insipidus, and hypoparathyroidism.
  • LISINOPRIL 20 mg/1 - One of the ANGIOTENSIN-CONVERTING ENZYME INHIBITORS (ACE inhibitors), orally active, that has been used in the treatment of hypertension and congestive heart failure.

Lisinopril And Hydrochlorothiazide Active Ingredients UNII Codes

NDC to RxNorm Crosswalk

What is RxNorm? 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: 197887 - lisinopril 20 MG / hydroCHLOROthiazide 25 MG Oral Tablet
  • RxCUI: 197887 - hydrochlorothiazide 25 MG / lisinopril 20 MG Oral Tablet
  • RxCUI: 197887 - HCTZ 25 MG / lisinopril 20 MG Oral Tablet

Lisinopril And Hydrochlorothiazide 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.

Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Lisinopril And Hydrochlorothiazide Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Package Label.Principal Display Panel



Lisinopril/ Hctz 20/25 mg Tablet


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