NDC 0536-1137

Mucus Relief D

Guaifenesin And Pseudoephedrine Hydrochloride

Mucus Relief D is a Oral Tablet, Extended Release in the Human Otc Drug category. It is labeled and distributed by Rugby Laboratories. The primary component is Guaifenesin; Pseudoephedrine Hydrochloride.

Product ID0536-1137_a0c55dff-f90c-4af5-ac04-6f09bbcb5827
NDC0536-1137
Product TypeHuman Otc Drug
Proprietary NameMucus Relief D
Generic NameGuaifenesin And Pseudoephedrine Hydrochloride
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2018-03-01
Marketing CategoryNDA / NDA
Application NumberNDA021585
Labeler NameRugby Laboratories
Substance NameGUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Active Ingredient Strength600 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0536-1137-21

1 BLISTER PACK in 1 CARTON (0536-1137-21) > 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing Start Date2018-03-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0536-1137-36 [00536113736]

Mucus Relief D TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021585
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-03-01

NDC 0536-1137-21 [00536113721]

Mucus Relief D TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021585
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-03-01

Drug Details

Active Ingredients

IngredientStrength
GUAIFENESIN600 mg/1

OpenFDA Data

SPL SET ID:f043ec98-6eb4-4c0c-b74c-56fdd867a520
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1305603

    • NDC Crossover Matching brand name "Mucus Relief D" or generic name "Guaifenesin And Pseudoephedrine Hydrochloride"

    NDCBrand NameGeneric Name
    0363-0144Mucus Relief DGuaifenesin, pseudoephedrine hydrochloride
    0363-0547Mucus Relief DGuaifenesin, Pseudoephedrine HCl
    0363-1604Mucus Relief DGuaifenesin and Pseudoephedrine HCL
    0363-7064Mucus Relief DGuaifenesin and Pseudoephedrine HCL
    0536-1137Mucus Relief DGuaifenesin and Pseudoephedrine Hydrochloride
    11822-0144mucus relief dGuaifenesin, pseudoephedrine hydrochloride
    11822-7399Mucus Relief DGuaifenesin and Pseudoephedrine HCL
    37808-446Mucus Relief DGuaifenesin, pseudoephedrine hydrochloride
    37808-777mucus relief dGuaifenesin, pseudoephedrine hydrochloride
    41250-547Mucus Relief DGuaifenesin, Pseudoephedrine HCl
    69842-211Mucus Relief DMucus Relief D
    0363-0077Guaifenesin and Pseudoephedrine HydrochlorideGuaifenesin and Pseudoephedrine Hydrochloride
    41415-994Guaifenesin and Pseudoephedrine HydrochlorideGuaifenesin and Pseudoephedrine Hydrochloride
    51660-071Guaifenesin and Pseudoephedrine HydrochlorideGuaifenesin and Pseudoephedrine Hydrochloride
    62011-0475Guaifenesin and Pseudoephedrine HydrochlorideGuaifenesin and Pseudoephedrine Hydrochloride
    0363-9930Guaifenesin DGuaifenesin and Pseudoephedrine Hydrochloride
    0536-1333Guaifenesin DGuaifenesin and Pseudoephedrine Hydrochloride
    51316-993Guaifenesin DGuaifenesin and Pseudoephedrine Hydrochloride
    58605-101MaxifedGUAIFENESIN and Pseudoephedrine Hydrochloride
    51316-970MAXIMUM STRENGTH Mucus Dguaifenesin and pseudoephedrine hydrochloride
    50090-1075Mucinex DGuaifenesin and Pseudoephedrine Hydrochloride
    50090-1076Mucinex DGuaifenesin and Pseudoephedrine Hydrochloride
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.