83059-0060
Generic: bismuth subsalicylate softgel
Labeler: shield pharmaceuticals corpDrug Facts
Product Profile
Brand Name
Generic Name
bismuth subsalicylate softgel
Labeler
shield pharmaceuticals corp
Dosage Form
CAPSULE, LIQUID FILLED
Active Ingredients
bismuth subsalicylate 262 mg/1
Identifiers & Regulatory
Product NDC
83059-0060
Product ID
83059-0060_4263d96a-d71f-3c17-e063-6294a90a400e
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
2024-12-11
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
830590060
Hyphenated Format
83059-0060
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
Generic Name
bismuth subsalicylate softgel (source: ndc)
Resolved Composition
Strengths
- 262 mg/1
Packaging
- 13500 CAPSULE, LIQUID FILLED in 1 DRUM (83059-0060-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "4263d96a-d71f-3c17-e063-6294a90a400e", "openfda": {}, "finished": false, "packaging": [{"description": "13500 CAPSULE, LIQUID FILLED in 1 DRUM (83059-0060-0)", "package_ndc": "83059-0060-0", "marketing_start_date": "11-DEC-24"}], "product_id": "83059-0060_4263d96a-d71f-3c17-e063-6294a90a400e", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "83059-0060", "generic_name": "Bismuth Subsalicylate Softgel", "labeler_name": "Shield Pharmaceuticals Corp", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "BISMUTH SUBSALICYLATE", "strength": "262 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20241211", "listing_expiration_date": "20261231"}