0078-0500 : Lamisil 187.5 mg/1 Oral Granule


NDC0078-0500
Labeler: Novartis Pharmaceuticals Corporation
Product Type: Human Prescription Drug
Drug Name:  Lamisil
Dosage Form: Oral Granule
Application #: NDA022071
Rev. Date: 


NDC Package Codes:

  • 0078-0500-58: 14 PACKET IN 1 CARTON (0078‑0500‑58) > 1 GRANULE IN 1 PACKET (0078‑0500‑62)
  • 0078-0500-59: 3 CARTON IN 1 PACKAGE (0078‑0500‑59) > 14 PACKET IN 1 CARTON (0078‑0500‑58) > 1 GRANULE IN 1 PACKET (0078‑0500‑62)

Active Ingredients:

  • Terbinafine Hydrochloride

Dosage Strength:

  • 187.5 mg

Pharmaceutical Classes:

  • Allylamine [Chemical/Ingredient]
  • Allylamine Antifungal [EPC]

Related Products:

Based on records with the same trade name.
  • 0078-0179 Lamisil (As Terbinafine Hydrochloride) 250 mg Oral Tablet by Novartis Pharmaceuticals Corporation
  • 0078-0499 Lamisil 125 mg/1 Oral Granule by Novartis Pharmaceuticals Corporation
  • 54868-6105 Lamisil 1.25 ml/125ml Topical Spray by Physicians Total Care, 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.