mucus relief

Generic: guaifenesin

Labeler: bi-mart
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin
Labeler bi-mart
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

guaifenesin 1200 mg/1

Manufacturer
Bi-Mart

Identifiers & Regulatory

Product NDC 37835-412
Product ID 37835-412_33d4125b-83ad-18f0-e063-6394a90a679d
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA213420
Listing Expiration 2026-12-31
Marketing Start 2020-12-18

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 37835412
Hyphenated Format 37835-412

Supplemental Identifiers

RxCUI
310621
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 (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number ANDA213420 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1200 mg/1
source: ndc
Packaging
  • 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (37835-412-28)
source: ndc

Packages (1)

37835-412-28 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (37835-412-28)

Ingredients (1)

guaifenesin (1200 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": "33d4125b-83ad-18f0-e063-6394a90a679d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["d995a6a5-d68b-44e4-9281-32c5417fb5e3"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Bi-Mart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (37835-412-28)", "package_ndc": "37835-412-28", "marketing_start_date": "20250401"}], "brand_name": "MUCUS RELIEF", "product_id": "37835-412_33d4125b-83ad-18f0-e063-6394a90a679d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "37835-412", "generic_name": "GUAIFENESIN", "labeler_name": "Bi-Mart", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCUS RELIEF", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20201218", "listing_expiration_date": "20261231"}