bexarotene
Generic: bexarotene
Labeler: upsher-smith laboratories, inc.Drug Facts
Product Profile
Brand Name
bexarotene
Generic Name
bexarotene
Labeler
upsher-smith laboratories, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
bexarotene 75 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0832-0285
Product ID
0832-0285_0392c67b-a83c-4e6c-95d6-09604953652d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209886
Listing Expiration
2026-12-31
Marketing Start
2018-07-25
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
08320285
Hyphenated Format
0832-0285
Supplemental Identifiers
RxCUI
UPC
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
bexarotene (source: ndc)
Generic Name
bexarotene (source: ndc)
Application Number
ANDA209886 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 75 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (0832-0285-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0392c67b-a83c-4e6c-95d6-09604953652d", "openfda": {"nui": ["N0000175607", "M0018962"], "upc": ["0308320285009"], "unii": ["A61RXM4375"], "rxcui": ["308725"], "spl_set_id": ["7437a43f-172a-4f4e-8132-fe23b00224f9"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Upsher-Smith Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0832-0285-00)", "package_ndc": "0832-0285-00", "marketing_start_date": "20180725"}], "brand_name": "Bexarotene", "product_id": "0832-0285_0392c67b-a83c-4e6c-95d6-09604953652d", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "0832-0285", "generic_name": "Bexarotene", "labeler_name": "Upsher-Smith Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bexarotene", "active_ingredients": [{"name": "BEXAROTENE", "strength": "75 mg/1"}], "application_number": "ANDA209886", "marketing_category": "ANDA", "marketing_start_date": "20180725", "listing_expiration_date": "20261231"}