albothyl
Generic: policresulen solution
Labeler: lydia co., ltd.Drug Facts
Product Profile
Brand Name
albothyl
Generic Name
policresulen solution
Labeler
lydia co., ltd.
Dosage Form
LIQUID
Routes
Active Ingredients
policresulen 720 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
72988-0035
Product ID
72988-0035_001d54ef-148b-e55a-e063-6294a90a7c40
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2023-01-23
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
729880035
Hyphenated Format
72988-0035
Supplemental Identifiers
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
albothyl (source: ndc)
Generic Name
policresulen solution (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 720 mg/g
Packaging
- 5 g in 1 BOTTLE (72988-0035-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "001d54ef-148b-e55a-e063-6294a90a7c40", "openfda": {"unii": ["6I19M5GB0G"], "spl_set_id": ["f2ea4e1b-a3d7-d063-e053-2a95a90a6d0b"], "manufacturer_name": ["Lydia Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 g in 1 BOTTLE (72988-0035-1)", "package_ndc": "72988-0035-1", "marketing_start_date": "20230123"}], "brand_name": "ALBOTHYL", "product_id": "72988-0035_001d54ef-148b-e55a-e063-6294a90a7c40", "dosage_form": "LIQUID", "product_ndc": "72988-0035", "generic_name": "Policresulen Solution", "labeler_name": "Lydia Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ALBOTHYL", "active_ingredients": [{"name": "POLICRESULEN", "strength": "720 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20230123", "listing_expiration_date": "20261231"}