major bismuth subsalicylate
Generic: bismuth subsalicylate
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
major bismuth subsalicylate
Generic Name
bismuth subsalicylate
Labeler
major pharmaceuticals
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
bismuth subsalicylate 262 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-7205
Product ID
0904-7205_61f89479-7da0-4f57-b505-d7ad3c2c52cb
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M008
Listing Expiration
2026-12-31
Marketing Start
2021-10-11
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047205
Hyphenated Format
0904-7205
Supplemental Identifiers
RxCUI
UNII
NUI
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
major bismuth subsalicylate (source: ndc)
Generic Name
bismuth subsalicylate (source: ndc)
Application Number
M008 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 262 mg/1
Packaging
- 5 BLISTER PACK in 1 BOX (0904-7205-46) / 6 TABLET, CHEWABLE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "61f89479-7da0-4f57-b505-d7ad3c2c52cb", "openfda": {"nui": ["M0002611", "N0000180183"], "unii": ["62TEY51RR1"], "rxcui": ["308761"], "spl_set_id": ["2a7c9cc1-206e-4018-b89d-7b634df43df6"], "pharm_class_cs": ["Bismuth [CS]"], "pharm_class_epc": ["Bismuth [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 BLISTER PACK in 1 BOX (0904-7205-46) / 6 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "0904-7205-46", "marketing_start_date": "20211011"}], "brand_name": "Major Bismuth Subsalicylate", "product_id": "0904-7205_61f89479-7da0-4f57-b505-d7ad3c2c52cb", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "0904-7205", "generic_name": "Bismuth subsalicylate", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Major Bismuth Subsalicylate", "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "application_number": "M008", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211011", "listing_expiration_date": "20261231"}