50991-510 : Duraflu Oral Tablet, Film Coated


NDC: 50991-510
Labeler: Poly Pharmaceuticals, Inc.
Product Type: Human OTC Drug
Drug Name:  Duraflu
Dosage Form: Oral Tablet, Film Coated
Application #: part341
Rev. Date: 


Appearance:


Markings: PE;723
Shapes:  Oval
Colors:  White
Size (mm): 20
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 50991-510-01: 100 TABLET, FILM COATED IN 1 BOTTLE (50991‑510‑01)
  • 50991-510-02: 12 BLISTER PACK IN 1 CARTON (50991‑510‑02) > 1 TABLET, FILM COATED IN 1 BLISTER PACK

Active Ingredients:

  • Acetaminophen
  • Dextromethorphan Hydrobromide
  • Guaifenesin
  • Pseudoephedrine Hydrochloride

Dosage Strength:

  • 500 mg
  • 20 mg
  • 200 mg
  • 60 mg

Inactive Ingredients:

  • Hypromelloses
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Carboxymethylcellulose Sodium
  • Silicon Dioxide
  • Stearic Acid

Related Products:

Based on records with the same trade name.
  • 50991-535 Duraflu Oral Tablet by Poly Pharmaceuticals, Inc.

NDC QR Code

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

NDC 50991-510 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.