0054-0177 NDC - BUPRENORPHINE HCL

Drug Information

Product NDC: 0054-0177

Proprietary Name: Buprenorphine HCl

Non Proprietary Name: Buprenorphine HCl

Active Ingredient(s):
  • 8 mg/1 BUPRENORPHINE HYDROCHLORIDE


Administration Route(s): SUBLINGUAL

Dosage Form(s): TABLET

Pharmacy Class(es):
  • Partial Opioid Agonist [EPC];
  • Partial Opioid Agonists [MoA]

Labeler Information

Labeler Name: Hikma Pharmaceuticals USA Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078633
Marketing Category: ANDA
Start Marketing Date:10/8/2009
DEA Schedule:CIII

Package Information

No. Package Code Package Description Billing Unit
10054-0177-1330 TABLET in 1 BOTTLE (0054-0177-13)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC0054-0177The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates 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.
PROPRIETARY NAMEBuprenorphine HClThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBuprenorphine HClThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe translation of the dosage form Code submitted by the firm.
ROUTE NAMESUBLINGUALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE10/8/2009This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct 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.
APPLICATION NUMBERANDA078633This 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.
LABELER NAMEHikma Pharmaceuticals USA Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEBUPRENORPHINE HYDROCHLORIDEThe following is the list of active ingredients in this product. 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.
ACTIVE NUMERATOR STRENGTH8 
ACTIVE INGRED UNITmg/1 
PHARM CLASSESPartial Opioid Agonist [EPC], Partial Opioid Agonists [MoA] 
DEA SCHEDULECIIIThis is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.

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This page was last updated on: 9/15/2022