70518-2824 : Siltussin Sa 100 mg/5ml Oral Liquid


NDC: 70518-2824
Labeler: Remedyrepack Inc.
Product Type: Human OTC Drug
Drug Name:  Siltussin Sa
Dosage Form: Oral Liquid
Application #: part341
Rev. Date: 


NDC Package Codes:

  • 70518-2824-0: 118 ML IN 1 BOTTLE, PLASTIC (70518‑2824‑0)
  • 70518-2824-1: 10 CUP, UNIT‑DOSE IN 1 BOX (70518‑2824‑1) > 20 ML IN 1 CUP, UNIT‑DOSE (70518‑2824‑2)

Active Ingredients:

  • Guaifenesin

Dosage Strength:

  • 100 mg/5mL

Pharmaceutical Classes:

  • Decreased Respiratory Secretion Viscosity [PE]
  • Expectorant [EPC]
  • Increased Respiratory Secretions [PE]

Related Products:

Based on records with the same trade name.
  • 17856-0117 Siltussin Sa 100 mg/5ml Oral Liquid by Atlantic Biologicals Corps
  • 50090-2675 Siltussin Sa 100 mg/5ml Oral Liquid by A-s Medication Solutions
  • 54838-117 Siltussin Sa 100 mg/5ml Oral Liquid by Silarx Pharmaceuticals, Inc
  • 63187-341 Siltussin Sa 100 mg/5ml Oral Liquid by Proficient Rx Lp
  • 68788-9098 Siltussin Sa 100 mg/5ml Oral Liquid by Preferred Pharmaceuticals, Inc

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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.