Package 0093-0812-05

Brand: nortriptyline hydrochloride

Generic: nortriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-0812-05
Digits Only 0093081205
Product NDC 0093-0812
Product ID 0093-0812_314d74dc-7394-40b9-be81-cb67b6e925a1
Description

500 CAPSULE in 1 BOTTLE (0093-0812-05)

Marketing

Marketing Status
Marketed Since 1995-04-06
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": "314d74dc-7394-40b9-be81-cb67b6e925a1", "openfda": {"upc": ["0300930811012", "0300930812019", "0300930810015", "0300930813016"], "unii": ["00FN6IH15D"], "rxcui": ["198045", "198046", "198047", "317136"], "spl_set_id": ["b58d473a-b19f-4d2a-b1ae-dd398d7a29e1"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0093-0812-01)", "package_ndc": "0093-0812-01", "marketing_start_date": "19950405"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (0093-0812-05)", "package_ndc": "0093-0812-05", "marketing_start_date": "19950406"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "0093-0812_314d74dc-7394-40b9-be81-cb67b6e925a1", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0093-0812", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA074132", "marketing_category": "ANDA", "marketing_start_date": "19950405", "listing_expiration_date": "20261231"}