NDC 0121-0744

GUAIFENESIN

Guaifenesin

GUAIFENESIN is a Oral Solution in the Human Otc Drug category. It is labeled and distributed by Pharmaceutical Associates, Inc.. The primary component is Guaifenesin.

Product ID0121-0744_63f0e37d-e6e4-dec5-e053-2991aa0a2244
NDC0121-0744
Product TypeHuman Otc Drug
Proprietary NameGUAIFENESIN
Generic NameGuaifenesin
Dosage FormSolution
Route of AdministrationORAL
Marketing Start Date2002-09-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NamePharmaceutical Associates, Inc.
Substance NameGUAIFENESIN
Active Ingredient Strength100 mg/5mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0121-0744-04

118 mL in 1 BOTTLE (0121-0744-04)
Marketing Start Date2002-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0121-0744-16 [00121074416]

GUAIFENESIN SOLUTION
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2002-09-01

NDC 0121-0744-04 [00121074404]

GUAIFENESIN SOLUTION
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2002-09-01

NDC 0121-0744-08 [00121074408]

GUAIFENESIN SOLUTION
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2002-09-01

Drug Details

Active Ingredients

IngredientStrength
GUAIFENESIN100 mg/5mL

OpenFDA Data

SPL SET ID:c2e53fb5-2798-47c8-9285-d1077d46e629
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310604

    • NDC Crossover Matching brand name "GUAIFENESIN" or generic name "Guaifenesin"

    NDCBrand NameGeneric Name
    0121-0744GUAIFENESINGUAIFENESIN
    0121-1488GUAIFENESINGUAIFENESIN
    0121-1744GUAIFENESINGUAIFENESIN
    0121-2232GUAIFENESINGUAIFENESIN
    0363-0028GuaifenesinGuaifenesin
    0363-0033GuaifenesinGuaifenesin
    70000-0106GuaifenesinGuaifenesin
    70518-1782GuaifenesinGuaifenesin
    0904-5154GuaifenesinGuaifenesin
    15338-769GuaifenesinGuaifenesin
    30142-703GuaifenesinGuaifenesin
    42291-313GuaifenesinGuaifenesin
    49349-511GuaifenesinGuaifenesin
    50383-063GuaifenesinGuaifenesin
    51660-070GUAIFENESINGUAIFENESIN
    55154-5780GUAIFENESINGUAIFENESIN
    55154-9437GuaifenesinGuaifenesin
    58657-509GuaifenesinGuaifenesin
    65162-037GuaifenesinGuaifenesin
    65162-036GuaifenesinGuaifenesin
    67046-251GuaifenesinGuaifenesin
    55154-9450GUAIFENESINGUAIFENESIN
    58602-810GuaifenesinGuaifenesin
    58602-811GuaifenesinGuaifenesin
    62207-569GUAIFENESINGUAIFENESIN
    79395-001GuaifenesinGuaifenesin
    69618-061GuaifenesinGuaifenesin
    58602-853GuaifenesinGuaifenesin
    63629-1156GuaifenesinGuaifenesin
    62207-839GUAIFENESINGUAIFENESIN
    62207-840GUAIFENESINGUAIFENESIN
    0363-0288childrens chest congestionGuaifenesin
    0113-0325Good Sense Mucus ERGuaifenesin
    0113-2023good sense mucus erguaifenesin
    0113-3650Good Sense Mucus ERGuaifenesin
    0113-0061good sense tussinGuaifenesin
    0363-0071MucusGuaifenesin
    0363-0074MucusGuaifenesin
    0363-0532Mucus ReliefGuaifenesin
    0363-0325mucus relief erGuaifenesin
    0031-9303Robitussin Direct Chest Congestionguaifenesin
    0031-8724Robitussin Mucus Plus Chest CongestionGuaifenesin
    0113-2061tussinGuaifenesin
    0363-0310wal tussinGuaifenesin
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.