54569-4392 : Guaifenesin Extended Release 600 mg Oral Tablet, Extended Release


NDC: 54569-4392
Labeler: A-s Medication Solutions
Product Type: Human OTC Drug
Drug Name:  Guaifenesin Extended Release
Dosage Form: Oral Tablet, Extended Release
Application #: ANDA078912
Rev. Date: 


NDC Package Codes:

  • 54569-4392-1: 20 TABLET, EXTENDED RELEASE IN 1 BOTTLE (54569‑4392‑1)
  • 54569-4392-2: 40 TABLET, EXTENDED RELEASE IN 1 BOTTLE (54569‑4392‑2)

Active Ingredients:

  • Guaifenesin

Dosage Strength:

  • 600 mg

Related Products:

Based on records with the same trade name.
  • 30142-962 Guaifenesin Extended Release 1200 mg Oral Tablet, Extended Release by Kroger Company
  • 41415-997 Guaifenesin Extended Release 1200 mg Oral Tablet, Extended Release by Publix Super Markets, Inc
  • 45802-325 Guaifenesin Extended Release Extended Release 1200 mg Oral Tablet, Extended Release by Perrigo New York Inc
  • 49035-074 Guaifenesin Extended Release 1200 mg Oral Tablet, Extended Release by Walmart Stores, Inc.
  • 49999-078 Guaifenesin Extended Release 600 mg Oral Tablet, Extended Release by Lake Erie Medical Dba Quality Care Products LLC
  • 51660-072 Guaifenesin Extended Release 1200 mg Oral Tablet, Extended Release by Ohm Laboratories Inc
  • 63868-390 Guaifenesin Extended Release 1200 mg Oral Tablet, Extended Release by Chain Drug Marketing Association Inc
  • 68094-048 Guaifenesin Extended-release Extended-release 600 mg Oral Tablet, Multilayer, Extended Release by Precision Dose Inc.
  • 68196-072 Guaifenesin Extended Release 1200 mg Oral Tablet, Extended Release by Sam's West Inc
  • 68196-996 Guaifenesin Extended Release 1200 mg Oral Tablet, Extended Release by Sam's West Inc
  • 69842-016 Guaifenesin Extended Release 1200 mg Oral Tablet, Extended Release by Cvs Pharmacy
  • 70391-233 Guaifenesin Extended-release Extended-release 600 mg Oral Tablet, Extended Release by Guardian Pharmaceuticals, LLC
  • 70391-234 Guaifenesin Extended-release Extended-release 1200 mg Oral Tablet, Extended Release by Guardian Pharmaceuticals, LLC

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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.