mucus relief dm extended release caplets
Generic: guaifenesin, dextromethorphan hbr
Labeler: atlantic biologicals corp.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
Active Ingredients
dextromethorphan hydrobromide 30 mg/1, guaifenesin 600 mg/1
Manufacturer
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
178561162
Hyphenated Format
17856-1162
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 30 mg/1
- 600 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (17856-1162-1) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Packages (1)
Ingredients (2)
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"}