78206-180 : Zocor 10 mg Oral Tablet, Film Coated


NDC: 78206-180
Labeler: Organon LLC
Product Type: Human Prescription Drug
Drug Name:  Zocor
Dosage Form: Oral Tablet, Film Coated
Application #: NDA019766
Rev. Date: 


NDC Package Codes:

  • 78206-180-01: 30 TABLET, FILM COATED IN 1 BOTTLE (78206‑180‑01)
  • 78206-180-02: 90 TABLET, FILM COATED IN 1 BOTTLE (78206‑180‑02)

Active Ingredients:

  • Simvastatin

Dosage Strength:

  • 10 mg

Pharmaceutical Classes:

  • HMG-CoA Reductase Inhibitor [EPC]
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 78206-179 Zocor 80 mg Oral Tablet, Film Coated by Organon LLC
  • 78206-181 Zocor 20 mg Oral Tablet, Film Coated by Organon LLC
  • 78206-182 Zocor 40 mg Oral Tablet, Film Coated by Organon LLC
  • 0006-0543 Zocor 80 mg Oral Tablet by Merck Sharp & Dohme Corp.
  • 0006-0726 Zocor 5 mg Oral Tablet by Merck Sharp & Dohme Corp.
  • 0006-0735 Zocor 10 mg Oral Tablet by Merck Sharp & Dohme Corp.
  • 0006-0740 Zocor 20 mg Oral Tablet by Merck Sharp & Dohme Corp.
  • 0006-0749 Zocor 40 mg Oral Tablet by Merck Sharp & Dohme Corp.
  • 49999-306 Zocor 20 mg Oral Tablet by Lake Erie Medical Surgical & Supply Dba Quality Care Products LLC

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.