guaifenesin and dextromethorphan hbr
Generic: guaifenesin and dextromethorphan hbr
Labeler: cvs pharmacyDrug Facts
Product Profile
Brand Name
guaifenesin and dextromethorphan hbr
Generic Name
guaifenesin and dextromethorphan hbr
Labeler
cvs pharmacy
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
dextromethorphan hydrobromide 30 mg/1, guaifenesin 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51316-009
Product ID
51316-009_2885f0f5-e5ad-b667-c442-753a48d3f900
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA217340
Listing Expiration
2026-12-31
Marketing Start
2023-08-15
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51316009
Hyphenated Format
51316-009
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
guaifenesin and dextromethorphan hbr (source: ndc)
Generic Name
guaifenesin and dextromethorphan hbr (source: ndc)
Application Number
ANDA217340 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
- 600 mg/1
Packaging
- 5 BLISTER PACK in 1 CARTON (51316-009-01) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2885f0f5-e5ad-b667-c442-753a48d3f900", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["7942eeae-0528-4416-bd2f-b05acc71c0a9"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 BLISTER PACK in 1 CARTON (51316-009-01) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "51316-009-01", "marketing_start_date": "20230815"}], "brand_name": "Guaifenesin and Dextromethorphan HBR", "product_id": "51316-009_2885f0f5-e5ad-b667-c442-753a48d3f900", "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": "51316-009", "generic_name": "Guaifenesin and Dextromethorphan HBR", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin and Dextromethorphan HBR", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA217340", "marketing_category": "ANDA", "marketing_start_date": "20230815", "listing_expiration_date": "20261231"}