mucus relief dm extended release caplets
Generic: guaifenesin, dextromethorphan hbr
Labeler: equate (wal-mart stores, inc.) (see also wal-mart inc)Drug Facts
Product Profile
Brand Name
mucus relief dm extended release caplets
Generic Name
guaifenesin, dextromethorphan hbr
Labeler
equate (wal-mart stores, inc.) (see also wal-mart inc)
Dosage Form
TABLET
Routes
Active Ingredients
dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
49035-824
Product ID
49035-824_db451e95-ffce-40bb-8763-72a250448e70
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA209692
Listing Expiration
2026-12-31
Marketing Start
2019-11-29
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49035824
Hyphenated Format
49035-824
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
- 1 BOTTLE, PLASTIC in 1 BOX (49035-824-28) / 28 TABLET in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "db451e95-ffce-40bb-8763-72a250448e70", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0681131296229"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["3850544d-0d25-429e-98a9-5c4ad6cfd222"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (49035-824-28) / 28 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "49035-824-28", "marketing_start_date": "20191129"}], "brand_name": "Mucus Relief DM Extended Release Caplets", "product_id": "49035-824_db451e95-ffce-40bb-8763-72a250448e70", "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": "49035-824", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)", "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": "20191129", "listing_expiration_date": "20261231"}