mucus dm
Generic: guaifenesin and dextromethorphan hbr
Labeler: amerisource bergenDrug Facts
Product Profile
Brand Name
mucus dm
Generic Name
guaifenesin and dextromethorphan hbr
Labeler
amerisource bergen
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
46122-420
Product ID
46122-420_ac2755dc-dd3b-4bce-a467-3063a10e1ead
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA206941
Listing Expiration
2026-12-31
Marketing Start
2017-08-07
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
46122420
Hyphenated Format
46122-420
Supplemental Identifiers
RxCUI
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 dm (source: ndc)
Generic Name
guaifenesin and dextromethorphan hbr (source: ndc)
Application Number
ANDA206941 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
- 1200 mg/1
Packaging
- 4 BLISTER PACK in 1 CARTON (46122-420-03) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
- 2 BLISTER PACK in 1 CARTON (46122-420-74) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ac2755dc-dd3b-4bce-a467-3063a10e1ead", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["bf4bcec8-7136-4ae7-a459-a30ee881b98d"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Amerisource Bergen"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (46122-420-03) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "46122-420-03", "marketing_start_date": "20180709"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (46122-420-74) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "46122-420-74", "marketing_start_date": "20170807"}], "brand_name": "Mucus DM", "product_id": "46122-420_ac2755dc-dd3b-4bce-a467-3063a10e1ead", "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": "46122-420", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "Amerisource Bergen", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA206941", "marketing_category": "ANDA", "marketing_start_date": "20170807", "listing_expiration_date": "20261231"}