supress dm

Generic: dextromethorphan hydrobromide, guaifenesin

Labeler: kramer novis
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name supress dm
Generic Name dextromethorphan hydrobromide, guaifenesin
Labeler kramer novis
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 5 mg/mL, guaifenesin 50 mg/mL

Manufacturer
KRAMER NOVIS

Identifiers & Regulatory

Product NDC 52083-058
Product ID 52083-058_974dbf24-7689-4e94-a535-d5b59c097406
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2013-10-02

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 52083058
Hyphenated Format 52083-058

Supplemental Identifiers

RxCUI
1439992
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 supress dm (source: ndc)
Generic Name dextromethorphan hydrobromide, guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
  • 50 mg/mL
source: ndc
Packaging
  • 30 mL in 1 BOTTLE (52083-058-01)
source: ndc

Packages (1)

Ingredients (2)

dextromethorphan hydrobromide (5 mg/mL) guaifenesin (50 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "974dbf24-7689-4e94-a535-d5b59c097406", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1439992"], "spl_set_id": ["7da0611e-729c-4cf8-88f3-f8877b9f5cfa"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["KRAMER NOVIS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (52083-058-01)", "package_ndc": "52083-058-01", "marketing_start_date": "20131002"}], "brand_name": "Supress DM", "product_id": "52083-058_974dbf24-7689-4e94-a535-d5b59c097406", "dosage_form": "SYRUP", "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": "52083-058", "generic_name": "dextromethorphan hydrobromide, guaifenesin", "labeler_name": "KRAMER NOVIS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Supress DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "5 mg/mL"}, {"name": "GUAIFENESIN", "strength": "50 mg/mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20131002", "listing_expiration_date": "20261231"}