mucus relief dm extended release caplets (0363-0733)

Drug Facts

Product Profile

Brand Name mucus relief dm extended release caplets

Generic Name guaifenesin, dextromethorphan hbr

Labeler walgreens

Dosage Form TABLET

Routes

ORAL

Active Ingredients

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

Manufacturer

Walgreens

Identifiers & Regulatory

Product NDC 0363-0733

Product ID 0363-0733_e89d2575-c3c1-4633-866c-cecba7d52370

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA209692

Marketing Start 2019-01-01

Marketing End 2027-01-01

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 03630733

Hyphenated Format 0363-0733

Supplemental Identifiers

RxCUI

1298324

UPC

0311917202600

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 mucus relief dm extended release caplets (source: ndc)

Generic Name guaifenesin, dextromethorphan hbr (source: ndc)

Application Number ANDA209692 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

30 mg/1
600 mg/1

source: ndc

Packaging

20 BLISTER PACK in 1 CARTON (0363-0733-20) / 1 TABLET in 1 BLISTER PACK
40 BLISTER PACK in 1 CARTON (0363-0733-40) / 1 TABLET in 1 BLISTER PACK

source: ndc

Packages (2)

0363-0733-20 20 BLISTER PACK in 1 CARTON (0363-0733-20) / 1 TABLET in 1 BLISTER PACK 0363-0733-40 40 BLISTER PACK in 1 CARTON (0363-0733-40) / 1 TABLET in 1 BLISTER PACK

Ingredients (2)

dextromethorphan hydrobromide (30 mg/1) guaifenesin (600 mg/1)

Linked Drug Pages (1)

Mucus Relief DM Extended Release Caplets ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "e89d2575-c3c1-4633-866c-cecba7d52370", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0311917202600"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["be5ab61a-abd6-4dee-9607-2f1e2c47b2dc"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (0363-0733-20)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0363-0733-20", "marketing_end_date": "20270101", "marketing_start_date": "20190101"}, {"sample": false, "description": "40 BLISTER PACK in 1 CARTON (0363-0733-40)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0363-0733-40", "marketing_end_date": "20270101", "marketing_start_date": "20190101"}], "brand_name": "Mucus Relief DM Extended Release Caplets", "product_id": "0363-0733_e89d2575-c3c1-4633-866c-cecba7d52370", "dosage_form": "TABLET", "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": "0363-0733", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM Extended Release Caplets", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA209692", "marketing_category": "ANDA", "marketing_end_date": "20270101", "marketing_start_date": "20190101"}