mucus relief dm extended release caplets
Generic: guaifenesin, dextromethorphan hbr
Labeler: quality choice (chain drug marketing association)Drug Facts
Product Profile
Brand Name
mucus relief dm extended release caplets
Generic Name
guaifenesin, dextromethorphan hbr
Labeler
quality choice (chain drug marketing association)
Dosage Form
TABLET
Routes
Active Ingredients
dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63868-870
Product ID
63868-870_63708ea4-8e73-41a7-9bb7-184d112f86be
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA209692
Listing Expiration
2026-12-31
Marketing Start
2018-12-31
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63868870
Hyphenated Format
63868-870
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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 extended release caplets (source: ndc)
Generic Name
guaifenesin, dextromethorphan hbr (source: ndc)
Application Number
ANDA209692 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
- 1200 mg/1
Packaging
- 14 BLISTER PACK in 1 CARTON (63868-870-14) / 1 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "63708ea4-8e73-41a7-9bb7-184d112f86be", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515997059"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["ee34af0f-61ba-49fa-81e0-20da4c582368"], "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)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 CARTON (63868-870-14) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "63868-870-14", "marketing_start_date": "20181231"}], "brand_name": "Mucus Relief DM Extended Release Caplets", "product_id": "63868-870_63708ea4-8e73-41a7-9bb7-184d112f86be", "dosage_form": "TABLET", "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": "63868-870", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "QUALITY CHOICE (Chain Drug Marketing Association)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM Extended Release Caplets", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA209692", "marketing_category": "ANDA", "marketing_start_date": "20181231", "listing_expiration_date": "20261231"}