Package 43063-877-90

Brand: duloxetine

Generic: duloxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-877-90
Digits Only 4306387790
Product NDC 43063-877
Product ID 43063-877_3285a9f3-82fd-8b46-e063-6294a90ab809
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-877-90)

Marketing

Marketing Status
Marketed Since 2018-08-06
Brand duloxetine
Generic duloxetine hydrochloride
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": "3285a9f3-82fd-8b46-e063-6294a90ab809", "openfda": {"upc": ["0343063877906"], "unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["696a345f-d70c-4ce8-94f7-a8a21f2d20f0"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-877-90)", "package_ndc": "43063-877-90", "marketing_start_date": "20180806"}], "brand_name": "Duloxetine", "product_id": "43063-877_3285a9f3-82fd-8b46-e063-6294a90ab809", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "43063-877", "generic_name": "Duloxetine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090778", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}