mucus relief extended-release

Generic: guaifenesin

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief extended-release
Generic Name guaifenesin
Labeler target corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 600 mg/1

Manufacturer
TARGET Corporation

Identifiers & Regulatory

Product NDC 11673-731
Product ID 11673-731_b1c80af5-0e18-4d85-bf7d-1933a1a03cc3
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207342
Listing Expiration 2026-12-31
Marketing Start 2018-07-11

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 11673731
Hyphenated Format 11673-731

Supplemental Identifiers

RxCUI
636522
UPC
0359726731409
UNII
495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

Packaging Origin

Original Packager
true

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 extended-release (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number ANDA207342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 20 BLISTER PACK in 1 CARTON (11673-731-20) / 1 TABLET in 1 BLISTER PACK
  • 40 BLISTER PACK in 1 CARTON (11673-731-40) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

11673-731-20 20 BLISTER PACK in 1 CARTON (11673-731-20) / 1 TABLET in 1 BLISTER PACK 11673-731-40 40 BLISTER PACK in 1 CARTON (11673-731-40) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

guaifenesin (600 mg/1)

Linked Drug Pages (1)

Mucus Relief Extended-Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b1c80af5-0e18-4d85-bf7d-1933a1a03cc3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0359726731409"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["e374e8de-1eff-4f70-8e01-08e0f56b9789"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["TARGET Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (11673-731-20)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "11673-731-20", "marketing_start_date": "20180711"}, {"sample": false, "description": "40 BLISTER PACK in 1 CARTON (11673-731-40)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "11673-731-40", "marketing_start_date": "20180711"}], "brand_name": "Mucus Relief Extended-Release", "product_id": "11673-731_b1c80af5-0e18-4d85-bf7d-1933a1a03cc3", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "11673-731", "generic_name": "Guaifenesin", "labeler_name": "TARGET Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Extended-Release", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_start_date": "20180711", "listing_expiration_date": "20261231"}