stona
Generic: acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride
Labeler: sato pharmaceutical co., ltd.Drug Facts
Product Profile
Brand Name
stona
Generic Name
acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride
Labeler
sato pharmaceutical co., ltd.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 162.5 mg/1, chlorpheniramine maleate 2 mg/1, dextromethorphan hydrobromide 10 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
49873-114
Product ID
49873-114_0b3faa58-6fca-f550-e063-6394a90ad361
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2004-09-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49873114
Hyphenated Format
49873-114
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
stona (source: ndc)
Generic Name
acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 162.5 mg/1
- 2 mg/1
- 10 mg/1
- 5 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (49873-114-01) / 24 TABLET in 1 BOTTLE
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0b3faa58-6fca-f550-e063-6394a90ad361", "openfda": {"upc": ["0349873002033"], "unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1245169"], "spl_set_id": ["8b89f50d-88f8-4773-92ea-5ada61766056"], "manufacturer_name": ["Sato Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49873-114-01) / 24 TABLET in 1 BOTTLE", "package_ndc": "49873-114-01", "marketing_start_date": "20040929"}], "brand_name": "Stona", "product_id": "49873-114_0b3faa58-6fca-f550-e063-6394a90ad361", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "49873-114", "generic_name": "acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride", "labeler_name": "Sato Pharmaceutical Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stona", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "162.5 mg/1"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "2 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040929", "listing_expiration_date": "20261231"}