37808-762 : Mucus Relief Extended Release 1200 mg Oral Tablet


NDC: 37808-762
Labeler: H E B
Product Type: Human OTC Drug
Drug Name:  Mucus Relief Extended Release Maximum Strength
Dosage Form: Oral Tablet
Application #: ANDA207342
Rev. Date: 


NDC Package Codes:

  • 37808-762-14: 1 BOTTLE, PLASTIC IN 1 BOX (37808‑762‑14) > 14 TABLET IN 1 BOTTLE, PLASTIC
  • 37808-762-42: 1 BOTTLE, PLASTIC IN 1 BOX (37808‑762‑42) > 42 TABLET IN 1 BOTTLE, PLASTIC

Active Ingredients:

  • Guaifenesin

Dosage Strength:

  • 1200 mg

Pharmaceutical Classes:

  • Decreased Respiratory Secretion Viscosity [PE]
  • Expectorant [EPC]
  • Increased Respiratory Secretions [PE]

Related Products:

Based on records with the same trade name.
  • 0363-0832 Mucus Relief Extended Release 1200 mg Oral Tablet by Walgreens
  • 55315-732 Mucus Relief Extended Release 1200 mg Oral Tablet by Freds Inc
  • 62011-0378 Mucus Relief Extended Release 1200 mg Oral Tablet by Mckesson (Health Mart)
  • 63868-872 Mucus Relief Extended Release 1200 mg Oral Tablet by Quality Choice (Chain Drug Marketing Association)
  • 69256-732 Mucus Relief Extended Release 1200 mg Oral Tablet by Harris Teeter, LLC
  • 69842-732 Mucus Relief Extended Release 1200 mg Oral Tablet by Cvs Pharmacy
  • 70000-0479 Mucus Relief Extended Release 1200 mg Oral Tablet by Cardinal Health (Leader) 70000

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.