amoxapine

Generic: amoxapine

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxapine
Generic Name amoxapine
Labeler actavis pharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amoxapine 25 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0591-5713
Product ID 0591-5713_40931661-1155-4850-baaa-227f066ed616
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072691
Listing Expiration 2027-12-31
Marketing Start 1992-08-28

Pharmacologic Class

Established (EPC)
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05915713
Hyphenated Format 0591-5713

Supplemental Identifiers

RxCUI
197363 197364 197365 197366
UNII
R63VQ857OT
NUI
N0000175752

Packaging Origin

Original Packager
true

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: ndc)
Generic Name amoxapine (source: ndc)
Application Number ANDA072691 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (0591-5713-01)
source: ndc

Packages (1)

0591-5713-01 100 TABLET in 1 BOTTLE, PLASTIC (0591-5713-01)

Ingredients (1)

amoxapine (25 mg/1)

Linked Drug Pages (1)

Amoxapine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40931661-1155-4850-baaa-227f066ed616", "openfda": {"nui": ["N0000175752"], "unii": ["R63VQ857OT"], "rxcui": ["197363", "197364", "197365", "197366"], "spl_set_id": ["a16297df-3158-48db-85e5-5cd506885556"], "pharm_class_epc": ["Tricyclic Antidepressant [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0591-5713-01)", "package_ndc": "0591-5713-01", "marketing_start_date": "19920828"}], "brand_name": "Amoxapine", "product_id": "0591-5713_40931661-1155-4850-baaa-227f066ed616", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0591-5713", "generic_name": "Amoxapine", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxapine", "active_ingredients": [{"name": "AMOXAPINE", "strength": "25 mg/1"}], "application_number": "ANDA072691", "marketing_category": "ANDA", "marketing_start_date": "19920828", "listing_expiration_date": "20271231"}