0591-5713
Generic: Amoxapine
Labeler: Actavis Pharma, Inc.Drug Facts
Product Profile
Brand Name
Generic Name
Amoxapine
Labeler
Actavis Pharma, Inc.
Dosage Form
TABLET
Active Ingredients
AMOXAPINE 25 mg/1
Identifiers & Regulatory
Product NDC
0591-5713
Product ID
0591-5713_3f43042e-047a-4467-9e44-1d6b70f2e54c
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
1992-08-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05915713
Hyphenated Format
0591-5713
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
amoxapine (source: label)
Generic Name
Amoxapine (source: ndc)
Application Number
ANDA072691 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 76900 TABLET in 1 BAG (0591-5713-00)
- 92304 TABLET in 1 CONTAINER (0591-5713-77)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "3f43042e-047a-4467-9e44-1d6b70f2e54c", "openfda": {}, "finished": false, "packaging": [{"description": "76900 TABLET in 1 BAG (0591-5713-00)", "package_ndc": "0591-5713-00", "marketing_start_date": "28-AUG-92"}, {"description": "92304 TABLET in 1 CONTAINER (0591-5713-77)", "package_ndc": "0591-5713-77", "marketing_start_date": "31-JUL-24"}], "product_id": "0591-5713_3f43042e-047a-4467-9e44-1d6b70f2e54c", "dosage_form": "TABLET", "product_ndc": "0591-5713", "generic_name": "Amoxapine", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "AMOXAPINE", "strength": "25 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "19920828", "listing_expiration_date": "20261231"}