mucus relief dm

Generic: guaifenesin dextromethorphan hbr

Labeler: quality choice (chain drug marketing association)
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm
Generic Name guaifenesin dextromethorphan hbr
Labeler quality choice (chain drug marketing association)
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1

Manufacturer
QUALITY CHOICE (Chain Drug Marketing Association)

Identifiers & Regulatory

Product NDC 83324-137
Product ID 83324-137_9ae44fe4-3ac0-41a7-b5df-565e83ee71fa
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA209692
Listing Expiration 2026-12-31
Marketing Start 2024-07-31

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 83324137
Hyphenated Format 83324-137

Supplemental Identifiers

RxCUI
1099074
UPC
0635515997059
UNII
9D2RTI9KYH 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

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 dm (source: ndc)
Generic Name guaifenesin dextromethorphan hbr (source: ndc)
Application Number ANDA209692 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
  • 1200 mg/1
source: ndc
Packaging
  • 14 BLISTER PACK in 1 CARTON (83324-137-14) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

83324-137-14 14 BLISTER PACK in 1 CARTON (83324-137-14) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

dextromethorphan hydrobromide (60 mg/1) guaifenesin (1200 mg/1)

Linked Drug Pages (1)

Mucus Relief DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9ae44fe4-3ac0-41a7-b5df-565e83ee71fa", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515997059"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["8c9909bc-48b8-41d7-afe8-123e611a1448"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["QUALITY CHOICE (Chain Drug Marketing Association)"]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 CARTON (83324-137-14)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "83324-137-14", "marketing_start_date": "20240731"}], "brand_name": "Mucus Relief DM", "product_id": "83324-137_9ae44fe4-3ac0-41a7-b5df-565e83ee71fa", "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": "83324-137", "generic_name": "Guaifenesin Dextromethorphan HBr", "labeler_name": "QUALITY CHOICE (Chain Drug Marketing Association)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA209692", "marketing_category": "ANDA", "marketing_start_date": "20240731", "listing_expiration_date": "20261231"}