guaifenesin and dextromethorphan hbr (51660-301)

Drug Facts

Product Profile

Brand Name guaifenesin and dextromethorphan hbr

Generic Name guaifenesin and dextromethorphan hbr

Labeler ohm laboratories inc

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

dextromethorphan hydrobromide 30 mg/1, guaifenesin 600 mg/1

Manufacturer

OHM LABORATORIES INC

Identifiers & Regulatory

Product NDC 51660-301

Product ID 51660-301_eb963e6d-d883-41dd-96ed-5284d105a8f4

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA214781

Listing Expiration 2026-12-31

Marketing Start 2021-07-01

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 51660301

Hyphenated Format 51660-301

Supplemental Identifiers

RxCUI

1298324

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 ANDA214781 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

30 mg/1
600 mg/1

source: ndc

Packaging

1 BLISTER PACK in 1 CARTON (51660-301-21) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
2 BLISTER PACK in 1 CARTON (51660-301-41) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

source: ndc

Packages (2)

51660-301-21 1 BLISTER PACK in 1 CARTON (51660-301-21) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 51660-301-41 2 BLISTER PACK in 1 CARTON (51660-301-41) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

dextromethorphan hydrobromide (30 mg/1) guaifenesin (600 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": "eb963e6d-d883-41dd-96ed-5284d105a8f4", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["f2eb5494-2672-444f-afa3-d1ef8ed1eaa1"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["OHM LABORATORIES INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (51660-301-21)  / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "51660-301-21", "marketing_start_date": "20210701"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (51660-301-41)  / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "51660-301-41", "marketing_start_date": "20210701"}], "brand_name": "Guaifenesin and Dextromethorphan HBr", "product_id": "51660-301_eb963e6d-d883-41dd-96ed-5284d105a8f4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "51660-301", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "OHM LABORATORIES INC", "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": "ANDA214781", "marketing_category": "ANDA", "marketing_start_date": "20210701", "listing_expiration_date": "20261231"}