NDC 49035-261

Guaifenesin 1200 mg and Pseudoephedrine HCl 120 mg

Guaifenesin And Pseudoephedrine Hcl

Guaifenesin 1200 mg and Pseudoephedrine HCl 120 mg is a Oral Tablet, Extended Release in the Human Otc Drug category. It is labeled and distributed by Wal-mart Stores, Inc.. The primary component is Guaifenesin; Pseudoephedrine Hydrochloride.

Product ID49035-261_9fdb4c64-4860-08bb-b754-3d3ba2c96fea
NDC49035-261
Product TypeHuman Otc Drug
Proprietary NameGuaifenesin 1200 mg and Pseudoephedrine HCl 120 mg
Generic NameGuaifenesin And Pseudoephedrine Hcl
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2020-04-03
Marketing CategoryANDA / ANDA
Application NumberANDA208369
Labeler NameWal-mart Stores, Inc.
Substance NameGUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Active Ingredient Strength1200 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 49035-261-12

2 BLISTER PACK in 1 CARTON (49035-261-12) > 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing Start Date2020-04-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49035-261-12 [49035026112]

Guaifenesin 1200 mg and Pseudoephedrine HCl 120 mg TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA208369
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-03

NDC 49035-261-24 [49035026124]

Guaifenesin 1200 mg and Pseudoephedrine HCl 120 mg TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA208369
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-04-03
Marketing End Date2020-04-03

Drug Details

Active Ingredients

IngredientStrength
GUAIFENESIN1200 mg/1

OpenFDA Data

SPL SET ID:f3933531-aa4d-cb67-1895-f2f14175f1d2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1244675
  • NDC Crossover Matching brand name "Guaifenesin 1200 mg and Pseudoephedrine HCl 120 mg" or generic name "Guaifenesin And Pseudoephedrine Hcl"

    NDCBrand NameGeneric Name
    49035-261Guaifenesin 1200 mg and Pseudoephedrine HCl 120 mgGuaifenesin and Pseudoephedrine HCL
    0363-0134Guaifenesin and Pseudoephedrine HClGuaifenesin and Pseudoephedrine HCl
    0363-9946Guaifenesin and Pseudoephedrine HClGuaifenesin and Pseudoephedrine HCl
    11822-0046Guaifenesin and Pseudoephedrine HClGuaifenesin and Pseudoephedrine HCL
    30142-137Guaifenesin and Pseudoephedrine HClGuaifenesin and Pseudoephedrine HCl
    51660-057Guaifenesin and Pseudoephedrine HClGuaifenesin and Pseudoephedrine HCl
    51660-058Guaifenesin and Pseudoephedrine HClGuaifenesin and Pseudoephedrine HCl
    55111-798Guaifenesin and Pseudoephedrine HCLGuaifenesin and Pseudoephedrine HCL
    55111-799Guaifenesin and Pseudoephedrine HCLGuaifenesin and Pseudoephedrine HCL
    58602-833Guaifenesin and Pseudoephedrine HClGuaifenesin and Pseudoephedrine HCl
    58602-834Guaifenesin and Pseudoephedrine HClGuaifenesin and Pseudoephedrine HCl
    70677-0110Guaifenesin and Pseudoephedrine HClGuaifenesin and Pseudoephedrine HCL
    79481-1002Guaifenesin and Pseudoephedrine HClGuaifenesin and Pseudoephedrine HCl
    0363-1604Mucus Relief DGuaifenesin and Pseudoephedrine HCL
    0363-7064Mucus Relief DGuaifenesin and Pseudoephedrine HCL
    11822-7399Mucus Relief DGuaifenesin and Pseudoephedrine HCL
    69842-211Mucus Relief DGuaifenesin and Pseudoephedrine HCL
    70000-0608Mucus Relief DGuaifenesin and Pseudoephedrine HCL
    50991-212Poly-Vent IRGuaifenesin and Pseudoephedrine HCl

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.