50991-132 : Polytussin Dm Oral Syrup


NDC: 50991-132
Labeler: Poly Pharmaceuticals, Inc.
Product Type: Human OTC Drug
Drug Name:  Polytussin Dm
Dosage Form: Oral Syrup
Application #: part341
Rev. Date: 


NDC Package Codes:

  • 50991-132-15: 15 ML IN 1 BOTTLE (50991‑132‑15)
  • 50991-132-16: 480 ML IN 1 BOTTLE (50991‑132‑16)

Active Ingredients:

  • Dextromethorphan Hydrobromide
  • Phenylephrine Hydrochloride
  • Pyrilamine Maleate

Dosage Strength:

  • 7.5 mg/5mL
  • 5 mg/5mL
  • 12.5 mg/5mL

Pharmaceutical Classes:

  • Adrenergic alpha1-Agonists [MoA]
  • Sigma-1 Agonist [EPC]
  • Sigma-1 Receptor Agonists [MoA]
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]
  • Uncompetitive NMDA Receptor Antagonists [MoA]
  • alpha-1 Adrenergic Agonist [EPC]

Related Products:

Based on records with the same trade name.
  • 50991-492 Polytussin Dm Oral Syrup by Poly Pharmaceuticals, Inc.
  • 50991-121 Polytussin Dm Oral Liquid by Poly Pharmaceuticals,

NDC QR Code

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NDC 50991-132 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.