0121-0809 : Guaifenesin Dm Oral Solution


NDC: 0121-0809
Labeler: Pharmaceutical Associates, Inc.
Product Type: Human OTC Drug
Drug Name:  Guaifenesin Dm
Dosage Form: Oral Solution
Application #: part341
Rev. Date: 


NDC Package Codes:

  • 0121-0809-04: 118 ML IN 1 BOTTLE (0121‑0809‑04)
  • 0121-0809-08: 237 ML IN 1 BOTTLE (0121‑0809‑08)

Active Ingredients:

  • Dextromethorphan
  • Guaifenesin

Dosage Strength:

  • 10 mg/5mL
  • 200 mg/5mL

Related Products:

Based on records with the same trade name.
  • 0121-0638 Guaifenesin Dm Oral Syrup by Pharmaceutical Associates, Inc.
  • 0121-1276 Guaifenesin Dm Oral Syrup by Pharmaceutical Associates, Inc.
  • 0121-4809 Guaifenesin Dm Oral Solution by Pharmaceutical Associates, Inc.
  • 43063-801 Guaifenesin Dm Oral Tablet by Pd-rx Pharmaceuticals, Inc.
  • 50090-2303 Guaifenesin Dm Oral Syrup by A-s Medication Solutions
  • 50090-3492 Guaifenesin Dm Oral Syrup by A-s Medication Solutions
  • 54868-1986 Guaifenesin Oral Syrup by Physicians Total Care, Inc.
  • 55154-5783 Guaifenesin Dm Oral Syrup by Cardinal Health
  • 55154-5785 Guaifenesin Dm Oral Syrup by Cardinal Health
  • 60687-817 Guaifenesin Dm Oral Syrup by American Health Packaging
  • 60687-828 Guaifenesin Dm Oral Syrup by American Health Packaging
  • 63739-505 Guaifenesin Dm Oral Syrup by Mckesson Corporation Dba Sky Packaging
  • 63739-506 Guaifenesin Dm Oral Syrup by Mckesson Corporation Dba Sky Packaging
  • 68752-012 Guaifenesin Dm Oral Tablet by Pd-rx Pharmaceuticals, Inc.

NDC QR Code

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NDC 0121-0809 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.