maximum strength mucus relief dm

Generic: guaifenesin and dextromethorphan hbr

Labeler: walgreen co.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strength mucus relief dm
Generic Name guaifenesin and dextromethorphan hbr
Labeler walgreen co.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

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

Manufacturer
WALGREEN CO.

Identifiers & Regulatory

Product NDC 0363-0510
Product ID 0363-0510_12933549-899f-44ac-be98-afc7feb3e95e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206941
Listing Expiration 2026-12-31
Marketing Start 2017-03-17

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 03630510
Hyphenated Format 0363-0510

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 maximum strength mucus relief dm (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
  • 2 BLISTER PACK in 1 CARTON (0363-0510-65) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 CARTON (0363-0510-70) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 6 BLISTER PACK in 1 CARTON (0363-0510-99) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (3)

0363-0510-65 2 BLISTER PACK in 1 CARTON (0363-0510-65) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 0363-0510-70 4 BLISTER PACK in 1 CARTON (0363-0510-70) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 0363-0510-99 6 BLISTER PACK in 1 CARTON (0363-0510-99) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

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

Linked Drug Pages (1)

Maximum Strength Mucus Relief DM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "12933549-899f-44ac-be98-afc7feb3e95e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["83483b91-77e5-42ca-a467-21312ef32d30"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["WALGREEN CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0363-0510-65)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0363-0510-65", "marketing_start_date": "20170317"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (0363-0510-70)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0363-0510-70", "marketing_start_date": "20170317"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (0363-0510-99)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0363-0510-99", "marketing_start_date": "20170317"}], "brand_name": "Maximum Strength Mucus Relief DM", "product_id": "0363-0510_12933549-899f-44ac-be98-afc7feb3e95e", "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": "0363-0510", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "WALGREEN CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Mucus Relief DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA206941", "marketing_category": "ANDA", "marketing_start_date": "20170317", "listing_expiration_date": "20261231"}