Package 72789-338-90

Brand: duloxetine

Generic: duloxetine
NDC Package

Package Facts

Identity

Package NDC 72789-338-90
Digits Only 7278933890
Product NDC 72789-338
Product ID 72789-338_47a99c63-9a99-5f97-e063-6294a90a3632
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-338-90)

Marketing

Marketing Status
Marketed Since 2023-07-28
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": "47a99c63-9a99-5f97-e063-6294a90a3632", "openfda": {"upc": ["0372789338903"], "unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["db85a82d-84f1-41c8-964b-ac94ae4d8e7b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-338-90)", "package_ndc": "72789-338-90", "marketing_start_date": "20230728"}], "brand_name": "Duloxetine", "product_id": "72789-338_47a99c63-9a99-5f97-e063-6294a90a3632", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72789-338", "generic_name": "Duloxetine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20170316", "listing_expiration_date": "20271231"}