NDC 11822-1014

acid relief

Famotidine

acid relief is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Rite Aid Corporation. The primary component is Famotidine.

Product ID11822-1014_29a6dae5-4a6f-4a9a-b281-088340cf52a0
NDC11822-1014
Product TypeHuman Otc Drug
Proprietary Nameacid relief
Generic NameFamotidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2022-03-31
Marketing CategoryANDA /
Application NumberANDA077351
Labeler NameRite Aid Corporation
Substance NameFAMOTIDINE
Active Ingredient Strength20 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 11822-1014-0

1 BOTTLE in 1 CARTON (11822-1014-0) > 50 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date2022-03-31
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "acid relief" or generic name "Famotidine"

NDCBrand NameGeneric Name
41250-891acid reliefacid relief
55312-950acid reliefacid relief
41250-252acid reliefacid relief
41250-577Acid ReliefAcid Relief
0363-0141Acid ControllerFamotidine
0363-0701Acid ControllerFamotidine
0363-1203acid controllerfamotidine
0113-7141basic care acid reducerFamotidine
0113-7194Basic Care famotidineFamotidine
0093-2748FamotidineFamotidine
0172-5728FamotidineFamotidine
0172-5729FamotidineFamotidine
0338-5197FamotidineFamotidine
0363-0036FamotidineFamotidine
0363-1899FamotidineFamotidine
0113-0141good sense acid reducerFamotidine
0113-0194Good Sense Acid ReducerFamotidine
0187-4420Pepcidfamotidine
0187-4440Pepcidfamotidine

Trademark Results [acid relief]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ACID RELIEF
ACID RELIEF
78100441 not registered Dead/Abandoned
Hornack, Janmarie
2001-12-31

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