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 1200 mg/1

Manufacturer
TARGET Corporation

Identifiers & Regulatory

Product NDC 11673-732
Product ID 11673-732_0624fe9f-c5f8-4fd0-becf-0efde9821b5f
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 11673732
Hyphenated Format 11673-732

Supplemental Identifiers

RxCUI
310621
UPC
0359726733144
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
  • 1200 mg/1
source: ndc
Packaging
  • 14 BLISTER PACK in 1 CARTON (11673-732-14) / 1 TABLET in 1 BLISTER PACK
  • 28 BLISTER PACK in 1 CARTON (11673-732-28) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

11673-732-14 14 BLISTER PACK in 1 CARTON (11673-732-14) / 1 TABLET in 1 BLISTER PACK 11673-732-28 28 BLISTER PACK in 1 CARTON (11673-732-28) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

guaifenesin (1200 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": "0624fe9f-c5f8-4fd0-becf-0efde9821b5f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0359726733144"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["e521e8e1-8227-451a-8858-01c26f6e0657"], "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": "14 BLISTER PACK in 1 CARTON (11673-732-14)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "11673-732-14", "marketing_start_date": "20180711"}, {"sample": false, "description": "28 BLISTER PACK in 1 CARTON (11673-732-28)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "11673-732-28", "marketing_start_date": "20180711"}], "brand_name": "Mucus Relief Extended Release", "product_id": "11673-732_0624fe9f-c5f8-4fd0-becf-0efde9821b5f", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "11673-732", "generic_name": "Guaifenesin", "labeler_name": "TARGET Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Extended Release", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_start_date": "20180711", "listing_expiration_date": "20261231"}