biocof
Generic: dextromethorphan hydrobromide, guaifenesin, phenylephrine hcl
Labeler: advanced generic corporationDrug Facts
Product Profile
Brand Name
biocof
Generic Name
dextromethorphan hydrobromide, guaifenesin, phenylephrine hcl
Labeler
advanced generic corporation
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/5mL, guaifenesin 400 mg/5mL, phenylephrine hydrochloride 10 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
45737-249
Product ID
45737-249_472ea774-30a5-89c8-e063-6394a90a0036
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2012-07-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
45737249
Hyphenated Format
45737-249
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
biocof (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/5mL
- 400 mg/5mL
- 10 mg/5mL
Packaging
- 473 mL in 1 BOTTLE (45737-249-16)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "472ea774-30a5-89c8-e063-6394a90a0036", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1091331"], "spl_set_id": ["6ae6a0cb-b4fc-4e7d-aefc-6a52ca1ae3d6"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Advanced Generic Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (45737-249-16)", "package_ndc": "45737-249-16", "marketing_start_date": "20120701"}], "brand_name": "Biocof", "product_id": "45737-249_472ea774-30a5-89c8-e063-6394a90a0036", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "45737-249", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine HCL", "labeler_name": "Advanced Generic Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Biocof", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120701", "listing_expiration_date": "20261231"}