50991-535 : Duraflu Oral Tablet


NDC: 50991-535
Labeler: Poly Pharmaceuticals, Inc.
Product Type: Human OTC Drug
Drug Name:  Duraflu
Dosage Form: Oral Tablet
Application #: part341
Rev. Date: 


Appearance:


Markings: PE;723
Shapes:  Oval
Colors:  White
Size (mm): 20
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

NDC Package Codes:

  • 50991-535-01: 100 TABLET IN 1 BOTTLE (50991‑535‑01)
  • 50991-535-02: 6 BLISTER PACK IN 1 CARTON (50991‑535‑02) > 2 TABLET IN 1 BLISTER PACK

Active Ingredients:

  • Acetaminophen
  • Dextromethorphan Hydrobromide
  • Guaifenesin
  • Pseudoephedrine Hydrochloride

Dosage Strength:

  • 325 mg
  • 20 mg
  • 200 mg
  • 60 mg

Inactive Ingredients:

  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Stearic Acid

Pharmaceutical Classes:

  • Adrenergic alpha-Agonists [MoA]
  • Decreased Respiratory Secretion Viscosity [PE]
  • Expectorant [EPC]
  • Increased Respiratory Secretions [PE]
  • Sigma-1 Agonist [EPC]
  • Sigma-1 Receptor Agonists [MoA]
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]
  • Uncompetitive NMDA Receptor Antagonists [MoA]
  • alpha-Adrenergic Agonist [EPC]

Related Products:

Based on records with the same trade name.
  • 50991-510 Duraflu Oral Tablet, Film Coated by Poly Pharmaceuticals, Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 50991-535 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.