Package 60760-401-30

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-401-30
Digits Only 6076040130
Product NDC 60760-401
Product ID 60760-401_7aca25ab-0978-371b-e053-2a91aa0a0fc0
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (60760-401-30)

Marketing

Marketing Status
Marketed Since 2017-12-15
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": "7aca25ab-0978-371b-e053-2a91aa0a0fc0", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198046"], "spl_set_id": ["6064b662-4dd6-39f1-e053-2a91aa0a4d59"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (60760-401-30)", "package_ndc": "60760-401-30", "marketing_start_date": "20171215"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "60760-401_7aca25ab-0978-371b-e053-2a91aa0a0fc0", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60760-401", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075520", "marketing_category": "ANDA", "marketing_start_date": "20171215", "listing_expiration_date": "20261231"}