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