Package 72189-634-30

Brand: duloxetine d/r

Generic: duloxetine d/r
NDC Package

Package Facts

Identity

Package NDC 72189-634-30
Digits Only 7218963430
Product NDC 72189-634
Product ID 72189-634_3ac53025-8a9a-31de-e063-6294a90a53d2
Description

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-634-30)

Marketing

Marketing Status
Marketed Since 2025-07-25
Brand duloxetine d/r
Generic duloxetine d/r
Sample Package No

Linked Drug Pages (1)

Duloxetine D/R ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ac53025-8a9a-31de-e063-6294a90a53d2", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["3ac53025-8a99-31de-e063-6294a90a53d2"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-634-30)", "package_ndc": "72189-634-30", "marketing_start_date": "20250725"}], "brand_name": "Duloxetine D/R", "product_id": "72189-634_3ac53025-8a9a-31de-e063-6294a90a53d2", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72189-634", "generic_name": "Duloxetine D/R", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine D/R", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20250725", "listing_expiration_date": "20261231"}