alvimopan
Generic: alvimopan
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
alvimopan
Generic Name
alvimopan
Labeler
actavis pharma, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
alvimopan 12 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0591-2312
Product ID
0591-2312_ef9ffdef-f019-4329-b6a4-658fa872d3b8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208295
Listing Expiration
2026-12-31
Marketing Start
2020-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05912312
Hyphenated Format
0591-2312
Supplemental Identifiers
RxCUI
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
alvimopan (source: ndc)
Generic Name
alvimopan (source: ndc)
Application Number
ANDA208295 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12 mg/1
Packaging
- 30 BLISTER PACK in 1 CARTON (0591-2312-15) / 1 CAPSULE in 1 BLISTER PACK (0591-2312-45)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef9ffdef-f019-4329-b6a4-658fa872d3b8", "openfda": {"unii": ["677C126AET"], "rxcui": ["799835"], "spl_set_id": ["2a0645b4-daf8-421f-b987-a4e478843c5d"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0591-2312-15) / 1 CAPSULE in 1 BLISTER PACK (0591-2312-45)", "package_ndc": "0591-2312-15", "marketing_start_date": "20201201"}], "brand_name": "Alvimopan", "product_id": "0591-2312_ef9ffdef-f019-4329-b6a4-658fa872d3b8", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0591-2312", "generic_name": "Alvimopan", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alvimopan", "active_ingredients": [{"name": "ALVIMOPAN", "strength": "12 mg/1"}], "application_number": "ANDA208295", "marketing_category": "ANDA", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}