Package 60760-838-30

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-838-30
Digits Only 6076083830
Product NDC 60760-838
Product ID 60760-838_35aa6dbf-04d9-6a1d-e063-6294a90a6afa
Description

30 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-838-30)

Marketing

Marketing Status
Marketed Since 2025-05-15
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Amitriptyline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35aa6dbf-04d9-6a1d-e063-6294a90a6afa", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["35aa7ab3-321a-97f7-e063-6294a90a91e2"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-838-30)", "package_ndc": "60760-838-30", "marketing_start_date": "20250515"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "60760-838_35aa6dbf-04d9-6a1d-e063-6294a90a6afa", "dosage_form": "TABLET, COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60760-838", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "20240520", "listing_expiration_date": "20261231"}