isotretinoin
Generic: isotretinoin
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
isotretinoin
Generic Name
isotretinoin
Labeler
actavis pharma, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
isotretinoin 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0591-2434
Product ID
0591-2434_2f164fd8-4912-4149-9292-0dc2249a69a3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205063
Listing Expiration
2026-12-31
Marketing Start
2021-04-29
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05912434
Hyphenated Format
0591-2434
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
isotretinoin (source: ndc)
Generic Name
isotretinoin (source: ndc)
Application Number
ANDA205063 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 3 BLISTER PACK in 1 CARTON (0591-2434-15) / 10 CAPSULE in 1 BLISTER PACK (0591-2434-45)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2f164fd8-4912-4149-9292-0dc2249a69a3", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["EH28UP18IF"], "rxcui": ["197843", "197844", "197845", "403930", "1547561", "1547565"], "spl_set_id": ["1cf11710-f966-4529-8e08-02175f588bca"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0591-2434-15) / 10 CAPSULE in 1 BLISTER PACK (0591-2434-45)", "package_ndc": "0591-2434-15", "marketing_start_date": "20210429"}], "brand_name": "Isotretinoin", "product_id": "0591-2434_2f164fd8-4912-4149-9292-0dc2249a69a3", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "0591-2434", "generic_name": "Isotretinoin", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isotretinoin", "active_ingredients": [{"name": "ISOTRETINOIN", "strength": "20 mg/1"}], "application_number": "ANDA205063", "marketing_category": "ANDA", "marketing_start_date": "20210429", "listing_expiration_date": "20261231"}