mucus dm

Generic: guaifenesin and dextromethorphan hbr

Labeler: amerisource bergen
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus dm
Generic Name guaifenesin and dextromethorphan hbr
Labeler amerisource bergen
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

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

Manufacturer
Amerisource Bergen

Identifiers & Regulatory

Product NDC 46122-420
Product ID 46122-420_ac2755dc-dd3b-4bce-a467-3063a10e1ead
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA206941
Listing Expiration 2026-12-31
Marketing Start 2017-08-07

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 46122420
Hyphenated Format 46122-420

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 mucus 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
  • 4 BLISTER PACK in 1 CARTON (46122-420-03) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (46122-420-74) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ac2755dc-dd3b-4bce-a467-3063a10e1ead", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["bf4bcec8-7136-4ae7-a459-a30ee881b98d"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Amerisource Bergen"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (46122-420-03)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "46122-420-03", "marketing_start_date": "20180709"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (46122-420-74)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "46122-420-74", "marketing_start_date": "20170807"}], "brand_name": "Mucus DM", "product_id": "46122-420_ac2755dc-dd3b-4bce-a467-3063a10e1ead", "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": "46122-420", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "Amerisource Bergen", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus 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": "20170807", "listing_expiration_date": "20261231"}