excaugh

Generic: guaifenesin

Labeler: fortune pharmacal company, limited
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name excaugh
Generic Name guaifenesin
Labeler fortune pharmacal company, limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 100 mg/1

Manufacturer
FORTUNE PHARMACAL COMPANY, LIMITED

Identifiers & Regulatory

Product NDC 51467-009
Product ID 51467-009_438103e3-da3d-16c8-e063-6394a90ad7f3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2016-04-26

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 51467009
Hyphenated Format 51467-009

Supplemental Identifiers

RxCUI
198687
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 excaugh (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 BOX (51467-009-01) / 12 TABLET in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 BOX (51467-009-02) / 12 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (1)

guaifenesin (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "438103e3-da3d-16c8-e063-6394a90ad7f3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["198687"], "spl_set_id": ["60803d28-ea6e-4ab9-9cc9-4909b4681ecd"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["FORTUNE PHARMACAL COMPANY, LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 BOX (51467-009-01)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "51467-009-01", "marketing_start_date": "20160426"}, {"sample": false, "description": "3 BLISTER PACK in 1 BOX (51467-009-02)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "51467-009-02", "marketing_start_date": "20180321"}], "brand_name": "EXCAUGH", "product_id": "51467-009_438103e3-da3d-16c8-e063-6394a90ad7f3", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "51467-009", "generic_name": "Guaifenesin", "labeler_name": "FORTUNE PHARMACAL COMPANY, LIMITED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EXCAUGH", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "100 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160426", "listing_expiration_date": "20261231"}