mucus relief extended release maximum strength

Generic: guaifenesin

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief extended release maximum strength
Generic Name guaifenesin
Labeler h e b
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 1200 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-762
Product ID 37808-762_caba79ca-704b-4d8d-a2e1-94a41da8593f
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207342
Listing Expiration 2026-12-31
Marketing Start 2021-08-02

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 37808762
Hyphenated Format 37808-762

Supplemental Identifiers

RxCUI
310621
UPC
0041220831906
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 maximum strength (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number ANDA207342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1200 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (37808-762-14) / 14 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 BOX (37808-762-42) / 42 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

37808-762-14 1 BOTTLE, PLASTIC in 1 BOX (37808-762-14) / 14 TABLET in 1 BOTTLE, PLASTIC 37808-762-42 1 BOTTLE, PLASTIC in 1 BOX (37808-762-42) / 42 TABLET in 1 BOTTLE, PLASTIC

Ingredients (1)

guaifenesin (1200 mg/1)

Linked Drug Pages (1)

Mucus Relief Extended Release Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "caba79ca-704b-4d8d-a2e1-94a41da8593f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041220831906"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["6f075c29-8256-4cac-96c4-a772a53ad21d"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-762-14)  / 14 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "37808-762-14", "marketing_start_date": "20210802"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-762-42)  / 42 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "37808-762-42", "marketing_start_date": "20210802"}], "brand_name": "Mucus Relief Extended Release Maximum Strength", "product_id": "37808-762_caba79ca-704b-4d8d-a2e1-94a41da8593f", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "37808-762", "generic_name": "Guaifenesin", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Extended Release", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_start_date": "20210802", "listing_expiration_date": "20261231"}