guaifenesin

Generic: guaifenesin

Labeler: bryant ranch prepack
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name guaifenesin
Generic Name guaifenesin
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 400 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-9616
Product ID 71335-9616_97d545be-a78d-48b5-b774-ded0e82d742f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-08-01

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713359616
Hyphenated Format 71335-9616

Supplemental Identifiers

RxCUI
359601
UNII
495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name guaifenesin (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (71335-9616-1)
  • 20 TABLET in 1 BOTTLE, PLASTIC (71335-9616-2)
  • 50 TABLET in 1 BOTTLE, PLASTIC (71335-9616-3)
  • 60 TABLET in 1 BOTTLE, PLASTIC (71335-9616-4)
  • 40 TABLET in 1 BOTTLE, PLASTIC (71335-9616-5)
source: ndc

Packages (5)

71335-9616-1 30 TABLET in 1 BOTTLE, PLASTIC (71335-9616-1) 71335-9616-2 20 TABLET in 1 BOTTLE, PLASTIC (71335-9616-2) 71335-9616-3 50 TABLET in 1 BOTTLE, PLASTIC (71335-9616-3) 71335-9616-4 60 TABLET in 1 BOTTLE, PLASTIC (71335-9616-4) 71335-9616-5 40 TABLET in 1 BOTTLE, PLASTIC (71335-9616-5)

Ingredients (1)

guaifenesin (400 mg/1)

Linked Drug Pages (1)

Guaifenesin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "97d545be-a78d-48b5-b774-ded0e82d742f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["570a71eb-2d19-4c7b-8c00-e1524bfa3844"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71335-9616-1)", "package_ndc": "71335-9616-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (71335-9616-2)", "package_ndc": "71335-9616-2", "marketing_start_date": "20221228"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (71335-9616-3)", "package_ndc": "71335-9616-3", "marketing_start_date": "20240403"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71335-9616-4)", "package_ndc": "71335-9616-4", "marketing_start_date": "20240403"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE, PLASTIC (71335-9616-5)", "package_ndc": "71335-9616-5", "marketing_start_date": "20240403"}], "brand_name": "Guaifenesin", "product_id": "71335-9616_97d545be-a78d-48b5-b774-ded0e82d742f", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "71335-9616", "generic_name": "Guaifenesin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}