dg health mucus dm
Generic: dextromethorphan hydrobromide, guaifenesin
Labeler: dolgencorp incDrug Facts
Product Profile
Brand Name
dg health mucus dm
Generic Name
dextromethorphan hydrobromide, guaifenesin
Labeler
dolgencorp inc
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
dextromethorphan hydrobromide 30 mg/1, guaifenesin 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55910-746
Product ID
55910-746_a95401cc-349e-435a-b953-4d8fd1f54744
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA207602
Listing Expiration
2026-12-31
Marketing Start
2023-01-26
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55910746
Hyphenated Format
55910-746
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
dg health mucus dm (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin (source: ndc)
Application Number
ANDA207602 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
- 600 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (55910-746-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE
- 6 BLISTER PACK in 1 CARTON (55910-746-91) / 1 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": "a95401cc-349e-435a-b953-4d8fd1f54744", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["a95401cc-349e-435a-b953-4d8fd1f54744"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Dolgencorp Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-746-01) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "55910-746-01", "marketing_start_date": "20230126"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (55910-746-91) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "55910-746-91", "marketing_start_date": "20230201"}], "brand_name": "DG health mucus dm", "product_id": "55910-746_a95401cc-349e-435a-b953-4d8fd1f54744", "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": "55910-746", "generic_name": "dextromethorphan hydrobromide, guaifenesin", "labeler_name": "Dolgencorp Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DG health mucus dm", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA207602", "marketing_category": "ANDA", "marketing_start_date": "20230126", "listing_expiration_date": "20261231"}