mucus relief dm extended release caplets

Generic: guaifenesin, dextromethorphan hbr

Labeler: atlantic biologicals corp.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief dm extended release caplets
Generic Name guaifenesin, dextromethorphan hbr
Labeler atlantic biologicals corp.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

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

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-1162
Product ID 17856-1162_3892f322-6fd8-1a19-e063-6394a90a70fe
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA209692
Listing Expiration 2026-12-31
Marketing Start 2018-12-13

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 178561162
Hyphenated Format 17856-1162

Supplemental Identifiers

RxCUI
1298324
UNII
9D2RTI9KYH 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

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
  • 100 BLISTER PACK in 1 CARTON (17856-1162-1) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3892f322-6fd8-1a19-e063-6394a90a70fe", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1298324"], "spl_set_id": ["308f50dd-e8d6-0264-e063-6394a90afa68"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (17856-1162-1)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "17856-1162-1", "marketing_start_date": "20250317"}], "brand_name": "Mucus Relief DM Extended Release Caplets", "product_id": "17856-1162_3892f322-6fd8-1a19-e063-6394a90a70fe", "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": "17856-1162", "generic_name": "Guaifenesin, Dextromethorphan HBr", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "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_start_date": "20181213", "listing_expiration_date": "20261231"}