mucus relief

Generic: guaifenesin

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin
Labeler bryant ranch prepack
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

guaifenesin 600 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2642
Product ID 71335-2642_bfd50410-1289-4b5d-86df-3b939d50bc27
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209215
Listing Expiration 2026-12-31
Marketing Start 2019-09-23

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 713352642
Hyphenated Format 71335-2642

Supplemental Identifiers

RxCUI
636522
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 mucus relief (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number ANDA209215 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-1)
  • 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-2)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-3)
  • 40 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-4)
  • 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-5)
  • 6 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-6)
source: ndc

Packages (6)

71335-2642-1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-1) 71335-2642-2 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-2) 71335-2642-3 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-3) 71335-2642-4 40 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-4) 71335-2642-5 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-5) 71335-2642-6 6 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-6)

Ingredients (1)

guaifenesin (600 mg/1)

Linked Drug Pages (1)

Mucus Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bfd50410-1289-4b5d-86df-3b939d50bc27", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["c648e711-e944-4574-83b3-ccce8732384e"], "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, EXTENDED RELEASE in 1 BOTTLE (71335-2642-1)", "package_ndc": "71335-2642-1", "marketing_start_date": "20250602"}, {"sample": false, "description": "20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-2)", "package_ndc": "71335-2642-2", "marketing_start_date": "20250602"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-3)", "package_ndc": "71335-2642-3", "marketing_start_date": "20250602"}, {"sample": false, "description": "40 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-4)", "package_ndc": "71335-2642-4", "marketing_start_date": "20250602"}, {"sample": false, "description": "14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-5)", "package_ndc": "71335-2642-5", "marketing_start_date": "20250602"}, {"sample": false, "description": "6 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-6)", "package_ndc": "71335-2642-6", "marketing_start_date": "20250602"}], "brand_name": "Mucus Relief", "product_id": "71335-2642_bfd50410-1289-4b5d-86df-3b939d50bc27", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "71335-2642", "generic_name": "Guaifenesin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA209215", "marketing_category": "ANDA", "marketing_start_date": "20190923", "listing_expiration_date": "20261231"}