robafen dm
Generic: dextromethorphan hydrobromide, guaifenesin
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
robafen dm
Generic Name
dextromethorphan hydrobromide, guaifenesin
Labeler
preferred pharmaceuticals inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 200 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8268
Product ID
68788-8268_95130e72-3bba-4927-b4fb-1f4f3cd8f65d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
part341
Listing Expiration
2026-12-31
Marketing Start
2022-09-23
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888268
Hyphenated Format
68788-8268
Supplemental Identifiers
RxCUI
UNII
NUI
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
robafen dm (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin (source: ndc)
Application Number
part341 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/20mL
- 200 mg/20mL
Packaging
- 1 BOTTLE in 1 CARTON (68788-8268-1) / 118 mL in 1 BOTTLE
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "95130e72-3bba-4927-b4fb-1f4f3cd8f65d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1790650"], "spl_set_id": ["5b2fd5ce-56ab-491a-81b9-44e35a5d2316"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68788-8268-1) / 118 mL in 1 BOTTLE", "package_ndc": "68788-8268-1", "marketing_start_date": "20220923"}], "brand_name": "robafen dm", "product_id": "68788-8268_95130e72-3bba-4927-b4fb-1f4f3cd8f65d", "dosage_form": "SOLUTION", "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": "68788-8268", "generic_name": "dextromethorphan hydrobromide, guaifenesin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "robafen dm", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/20mL"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220923", "listing_expiration_date": "20261231"}