11822-6123 : Acid Relief 20 mg Oral Tablet, Film Coated


NDC: 11822-6123
Labeler: Rite Aid Corporation
Product Type: Human OTC Drug
Drug Name:  Acid Relief
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA077351
Rev. Date: 


NDC Package Codes:

  • 11822-6123-0: 1 BOTTLE IN 1 CARTON (11822‑6123‑0) / 50 TABLET, FILM COATED IN 1 BOTTLE

Active Ingredients:

  • Famotidine

Dosage Strength:

  • 20 mg

Pharmaceutical Classes:

  • Histamine H2 Receptor Antagonists [MoA]
  • Histamine-2 Receptor Antagonist [EPC]

Related Products:

Based on records with the same trade name.
  • 11822-1014 Acid Relief 20 mg Oral Tablet, Film Coated by Rite Aid Corporation
  • 11822-1194 Acid Relief 20 mg Oral Tablet, Film Coated by Rite Aid Corporation
  • 11822-6141 Acid Relief 10 mg Oral Tablet, Film Coated by Rite Aid Corporation
  • 41250-252 Acid Relief 75 mg Oral Tablet, Coated by Meijer Distribution Inc
  • 41250-577 Acid Relief 150 mg Oral Tablet, Film Coated by Meijer Distribution Inc
  • 41250-891 Acid Relief 150 mg Oral Tablet, Film Coated by Meijer Distribution Inc
  • 55312-271 Ranitidine 75 mg (As Ranitidine Hydrochloride 84 mg) Oral Tablet by Western Family Foods Inc
  • 55312-852 Acid Relief 150 mg/1 Oral Tablet, Film Coated by Western Family Foods Inc
  • 55312-950 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by Western Family Foods Inc

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.