amoxapine

Generic: amoxapine

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxapine
Generic Name amoxapine
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amoxapine 150 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-703
Product ID 62135-703_298fbb0d-737b-b42f-e063-6394a90ac69b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072879
Listing Expiration 2026-12-31
Marketing Start 1991-06-28

Pharmacologic Class

Established (EPC)
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135703
Hyphenated Format 62135-703

Supplemental Identifiers

RxCUI
197363 197364 197365 197366
UPC
0362135702908 0362135701901 0362135700904 0362135703301
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 ANDA072879 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (62135-703-30)
source: ndc

Packages (1)

62135-703-30 30 TABLET in 1 BOTTLE (62135-703-30)

Ingredients (1)

amoxapine (150 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": "298fbb0d-737b-b42f-e063-6394a90ac69b", "openfda": {"nui": ["N0000175752"], "upc": ["0362135702908", "0362135701901", "0362135700904", "0362135703301"], "unii": ["R63VQ857OT"], "rxcui": ["197363", "197364", "197365", "197366"], "spl_set_id": ["eed5e856-dd7b-4eaa-9dad-508f2bef9328"], "pharm_class_epc": ["Tricyclic Antidepressant [EPC]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62135-703-30)", "package_ndc": "62135-703-30", "marketing_start_date": "20230906"}], "brand_name": "Amoxapine", "product_id": "62135-703_298fbb0d-737b-b42f-e063-6394a90ac69b", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "62135-703", "generic_name": "Amoxapine", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxapine", "active_ingredients": [{"name": "AMOXAPINE", "strength": "150 mg/1"}], "application_number": "ANDA072879", "marketing_category": "ANDA", "marketing_start_date": "19910628", "listing_expiration_date": "20261231"}