up and up maximum strength mucus relief dm

Generic: dextromethorphan hydrobromide, guaifenesin

Labeler: Target Corporation
NDC Directory HUMAN OTC DRUG ANDA Active

Drug Facts

Product Profile

Brand Name up and up maximum strength mucus relief dm
Generic Name dextromethorphan hydrobromide, guaifenesin
Labeler Target Corporation
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

DEXTROMETHORPHAN HYDROBROMIDE 60 mg/1, GUAIFENESIN 1200 mg/1

Identifiers & Regulatory

Product NDC 11673-235
Product ID 11673-235_617ebd8b-85db-4a79-a9b3-877f77ffa75b
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207602
Listing Expiration 2026-12-31
Marketing Start 2018-09-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673235
Hyphenated Format 11673-235

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 up and up maximum strength mucus relief dm (source: ndc)
Generic Name dextromethorphan hydrobromide, guaifenesin (source: ndc)
Application Number ANDA207602 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
  • 1200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (11673-235-30) / 28 TABLET, EXTENDED RELEASE in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11673-235-55) / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11673-235-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
source: ndc

Packages (3)

11673-235-30 1 BOTTLE in 1 CARTON (11673-235-30) / 28 TABLET, EXTENDED RELEASE in 1 BOTTLE 11673-235-55 1 BOTTLE in 1 CARTON (11673-235-55) / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE 11673-235-66 1 BOTTLE in 1 CARTON (11673-235-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE

Ingredients (2)

DEXTROMETHORPHAN HYDROBROMIDE (60 mg/1) GUAIFENESIN (1200 mg/1)

Linked Drug Pages (1)

up and up maximum strength mucus relief dm ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "617ebd8b-85db-4a79-a9b3-877f77ffa75b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["5bcb49ee-94c2-4624-824a-84213ab152b1"], "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": "1 BOTTLE in 1 CARTON (11673-235-30)  / 28 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11673-235-30", "marketing_start_date": "20180927"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-235-55)  / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11673-235-55", "marketing_start_date": "20200417"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-235-66)  / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11673-235-66", "marketing_start_date": "20180927"}], "brand_name": "up and up maximum strength mucus relief dm", "product_id": "11673-235_617ebd8b-85db-4a79-a9b3-877f77ffa75b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "11673-235", "generic_name": "dextromethorphan hydrobromide, guaifenesin", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up maximum strength mucus relief dm", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA207602", "marketing_category": "ANDA", "marketing_start_date": "20180927", "listing_expiration_date": "20261231"}