Package 60687-900-01

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-900-01
Digits Only 6068790001
Product NDC 60687-900
Product ID 60687-900_44e5c7ee-ebf1-485a-e063-6294a90acb29
Description

100 BLISTER PACK in 1 CARTON (60687-900-01) / 1 CAPSULE in 1 BLISTER PACK (60687-900-11)

Marketing

Marketing Status
Marketed Since 2025-12-01
Brand nortriptyline hydrochloride
Generic nortriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Nortriptyline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "44e5c7ee-ebf1-485a-e063-6294a90acb29", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198045", "317136"], "spl_set_id": ["d111c36d-98ed-4f0d-97ea-86fe9048deee"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-900-01)  / 1 CAPSULE in 1 BLISTER PACK (60687-900-11)", "package_ndc": "60687-900-01", "marketing_start_date": "20251201"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "60687-900_44e5c7ee-ebf1-485a-e063-6294a90acb29", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60687-900", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA074132", "marketing_category": "ANDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}