Package 70518-4330-0

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4330-0
Digits Only 7051843300
Product NDC 70518-4330
Product ID 70518-4330_40300c18-032d-bcaf-e063-6294a90af7a8
Description

90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4330-0)

Marketing

Marketing Status
Marketed Since 2025-04-16
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40300c18-032d-bcaf-e063-6294a90af7a8", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["c072c1b3-ed8a-4f1e-ba6c-580a2b2c8f58"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4330-0)", "package_ndc": "70518-4330-0", "marketing_start_date": "20250416"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70518-4330_40300c18-032d-bcaf-e063-6294a90af7a8", "dosage_form": "TABLET, COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4330", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA212654", "marketing_category": "ANDA", "marketing_start_date": "20250416", "listing_expiration_date": "20261231"}