0031-8765 : Robitussin Maximum Strength 12 Hour Cough and Mucus Relief Oral Tablet, Extended Release


NDC0031-8765
Labeler: Wyeth Consumer Healthcare LLC
Product Type: Human OTC Drug
Drug Name:  Robitussin Maximum Strength 12 Hour Cough and Mucus Relief
Dosage Form: Oral Tablet, Extended Release
Application #: ANDA207602
Rev. Date: 


Appearance:


Markings: 2424
Shapes:  Oval
Colors:  Yellow
Size (mm): 22
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:

  • 0031-8765-04: 1 BLISTER PACK IN 1 CARTON (0031‑8765‑04) > 4 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
  • 0031-8765-08: 1 BLISTER PACK IN 1 CARTON (0031‑8765‑08) > 8 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
  • 0031-8765-16: 2 BLISTER PACK IN 1 CARTON (0031‑8765‑16) > 8 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK

Active Ingredients:

  • Dextromethorphan Hydrobromide
  • Guaifenesin

Dosage Strength:

  • 60 mg
  • 1200 mg

Inactive Ingredients:

  • Carbomer Homopolymer Type B (Allyl Pentaerythritol Or Allyl Sucrose Crosslinked)
  • Copovidone K25-31
  • D&c Yellow No. 10
  • Hypromellose, Unspecified
  • Magnesium Hydroxide
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Silicon Dioxide /

Pharmaceutical Classes:

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

NDC QR Code

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NDC 0031-8765 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.