50991-510 : Duraflu Oral Tablet, Film Coated


NDC50991-510
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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