up and up maximum strength mucus relief dm

Generic: dextromethorphan hydrobromide, guaifenesin

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

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

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-235
Product ID 11673-235_8d1e40fb-a9e8-46ca-9231-a6b61dace485
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207602
Marketing Start 2018-09-27
Marketing End 2026-04-30

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 11673235
Hyphenated Format 11673-235

Supplemental Identifiers

RxCUI
1099074
UNII
9D2RTI9KYH 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 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 (11673-235-55) / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE
source: ndc

Packages (1)

11673-235-55 1 BOTTLE in 1 CARTON (11673-235-55) / 42 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": "8d1e40fb-a9e8-46ca-9231-a6b61dace485", "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 (11673-235-55)  / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11673-235-55", "marketing_end_date": "20260430", "marketing_start_date": "20200417"}], "brand_name": "up and up maximum strength mucus relief dm", "product_id": "11673-235_8d1e40fb-a9e8-46ca-9231-a6b61dace485", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "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_end_date": "20260430", "marketing_start_date": "20180927"}