0536-1213 NDC - MUCUS RELIEF DM EXTENDED RELEASE CAPLETS (GUAIFENESIN, DEXTROMETHORPHAN HBR)

Drug Information

Product NDC: 0536-1213

Proprietary Name: Mucus Relief DM Extended Release Caplets

Non Proprietary Name: Guaifenesin, Dextromethorphan HBr

Active Ingredient(s):
  • 60 mg/1 DEXTROMETHORPHAN HYDROBROMIDE;
  • 1200 mg/1 GUAIFENESIN


Administration Route(s): ORAL

Dosage Form(s): TABLET

Pharmacy Class(es):
  • Decreased Respiratory Secretion Viscosity [PE];
  • Expectorant [EPC];
  • Increased Respiratory Secretions [PE];
  • Sigma-1 Agonist [EPC];
  • Sigma-1 Receptor Agonists [MoA];
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC];
  • Uncompetitive NMDA Receptor Antagonists [MoA]

Labeler Information

Labeler Name: Rugby Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA209692
Marketing Category: ANDA
Start Marketing Date:11/5/2018

Package Information

No. Package Code Package Description Billing Unit
10536-1213-8814 BLISTER PACK in 1 CARTON (0536-1213-88) / 1 TABLET in 1 BLISTER PACKEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC0536-1213The 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 OTC 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 NAMEMucus Relief DM Extended Release CapletsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEGuaifenesin, Dextromethorphan HBrThe 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 NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/5/2018This 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 NUMBERANDA209692This 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 NAMERugby Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEDEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESINAn 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 STRENGTH60; 1200 
ACTIVE INGRED UNITmg/1; mg/1 
PHARM CLASSESDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] 

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This page was last updated on: 2/1/2023