Package 71205-602-90

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 71205-602-90
Digits Only 7120560290
Product NDC 71205-602
Product ID 71205-602_f73fb658-ff2c-4847-a1ee-e551d2776f52
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-90)

Marketing

Marketing Status
Marketed Since 2021-08-20
Brand duloxetine
Generic duloxetine
Sample Package No

Linked Drug Pages (1)

Duloxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f73fb658-ff2c-4847-a1ee-e551d2776f52", "openfda": {"upc": ["0371205602604"], "unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["39bb9e78-e550-4bf9-ba6a-b4d9c7beaeb7"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-30)", "package_ndc": "71205-602-30", "marketing_start_date": "20210820"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-60)", "package_ndc": "71205-602-60", "marketing_start_date": "20210820"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-90)", "package_ndc": "71205-602-90", "marketing_start_date": "20210820"}], "brand_name": "Duloxetine", "product_id": "71205-602_f73fb658-ff2c-4847-a1ee-e551d2776f52", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71205-602", "generic_name": "Duloxetine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20170316", "listing_expiration_date": "20261231"}