0093-8107 : Ibuprofen and Famotidine Oral Tablet, Film Coated


NDC: 0093-8107
Labeler: Teva Pharmaceuticals USA, Inc.
Product Type: Human Prescription Drug
Drug Name:  Ibuprofen and Famotidine
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA211278
Rev. Date: 


NDC Package Codes:

  • 0093-8107-98: 90 TABLET, FILM COATED IN 1 BOTTLE (0093‑8107‑98)

Active Ingredients:

  • Ibuprofen
  • Famotidine

Dosage Strength:

  • 800 mg
  • 26.6 mg

Pharmaceutical Classes:

  • Anti-Inflammatory Agents
  • Non-Steroidal [CS]
  • Cyclooxygenase Inhibitors [MoA]
  • Histamine H2 Receptor Antagonists [MoA]
  • Histamine-2 Receptor Antagonist [EPC]
  • Nonsteroidal Anti-inflammatory Drug [EPC]

Related Products:

Based on records with the same trade name.
  • 31722-315 Ibuprofen and Famotidine Oral Tablet by Camber Pharmaceuticals, Inc.
  • 43602-544 Ibuprofen and Famotidine Oral Tablet by Ascent Pharmaceuticals, Inc.
  • 63629-8891 Ibuprofen and Famotidine Oral Tablet, Film Coated by Bryant Ranch Prepack
  • 67877-626 Ibuprofen and Famotidine Oral Tablet, Film Coated by Ascend Laboratories, LLC
  • 69306-266 Ibuprofen and Famotidine Oral Tablet, Film Coated by Doc Rx
  • 70748-312 Ibuprofen and Famotidine Oral Tablet, Coated by Lupin Pharmaceuticals, 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.