NDC 21130-399

MUCUS RELIEF MAX

Guaifenesin

MUCUS RELIEF MAX is a Oral Tablet, Extended Release in the Human Otc Drug category. It is labeled and distributed by Better Living Brands, Llc. The primary component is Guaifenesin.

Product ID21130-399_1ca7b7f8-8dd1-458d-ba23-b8ba742b8b5a
NDC21130-399
Product TypeHuman Otc Drug
Proprietary NameMUCUS RELIEF MAX
Generic NameGuaifenesin
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2020-07-17
Marketing CategoryANDA / ANDA
Application NumberANDA210453
Labeler NameBetter Living Brands, LLC
Substance NameGUAIFENESIN
Active Ingredient Strength1200 mg/1
Pharm ClassesDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 21130-399-01

1 BLISTER PACK in 1 CARTON (21130-399-01) > 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing Start Date2020-07-17
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "MUCUS RELIEF MAX" or generic name "Guaifenesin"

NDCBrand NameGeneric Name
21130-206Mucus Relief MaxMucus Relief Max
21130-399MUCUS RELIEF MAXMUCUS RELIEF MAX
0363-0288childrens chest congestionGuaifenesin
0113-0325Good Sense Mucus ERGuaifenesin
0113-2023good sense mucus erguaifenesin
0113-3650Good Sense Mucus ERGuaifenesin
0113-0061good sense tussinGuaifenesin
0121-0744GUAIFENESINGUAIFENESIN
0121-1488GUAIFENESINGUAIFENESIN
0121-1744GUAIFENESINGUAIFENESIN
0121-2232GUAIFENESINGUAIFENESIN
0363-0028GuaifenesinGuaifenesin
0363-0033GuaifenesinGuaifenesin
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.