guaifenesin and dextromethorphan hbr (71179-011)

Drug Facts

Product Profile

Brand Name guaifenesin and dextromethorphan hbr

Generic Name guaifenesin and dextromethorphan hbr

Labeler vespyr brands, inc.

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

dextromethorphan hydrobromide 60 mg/1, guaifenesin 1200 mg/1

Manufacturer

VESPYR BRANDS, INC.

Identifiers & Regulatory

Product NDC 71179-011

Product ID 71179-011_5ef449dd-0d48-4be9-b388-1cf47b170af3

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA206941

Listing Expiration 2026-12-31

Marketing Start 2022-07-14

Pharmacologic Class

Established (EPC)

expectorant [epc]

Physiologic Effect

decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71179011

Hyphenated Format 71179-011

Supplemental Identifiers

RxCUI

1099074

UNII

9D2RTI9KYH 495W7451VQ

NUI

N0000193956 N0000008867 N0000009560

Packaging Origin

Original Packager

true

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 ANDA206941 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

60 mg/1
1200 mg/1

source: ndc

Packaging

3 BLISTER PACK in 1 CARTON (71179-011-21) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

source: ndc

Packages (1)

71179-011-21 3 BLISTER PACK in 1 CARTON (71179-011-21) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

dextromethorphan hydrobromide (60 mg/1) guaifenesin (1200 mg/1)

Linked Drug Pages (1)

Guaifenesin and Dextromethorphan HBr ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "5ef449dd-0d48-4be9-b388-1cf47b170af3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["1c8fbf40-17c1-4ee9-a2b9-ca4a08e08293"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["VESPYR BRANDS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (71179-011-21)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "71179-011-21", "marketing_start_date": "20220714"}], "brand_name": "Guaifenesin and Dextromethorphan HBr", "product_id": "71179-011_5ef449dd-0d48-4be9-b388-1cf47b170af3", "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": "71179-011", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "VESPYR BRANDS, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin and Dextromethorphan HBr", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA206941", "marketing_category": "ANDA", "marketing_start_date": "20220714", "listing_expiration_date": "20261231"}