Duloxetine Delayed-Release

Generic: DULOXETINE HYDROCHLORIDE

Labeler: Golden State Medical Supply, Inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Duloxetine Delayed-Release
Generic Name DULOXETINE HYDROCHLORIDE
Labeler Golden State Medical Supply, Inc.
Dosage Form CAPSULE, DELAYED RELEASE PELLETS
Routes
ORAL
Active Ingredients

DULOXETINE HYDROCHLORIDE 30 mg/1

Identifiers & Regulatory

Product NDC 60429-165
Product ID 60429-165_3a8cefd0-9db7-8cd0-e063-6394a90a5996
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203088
Marketing Start 2014-06-11
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60429165
Hyphenated Format 60429-165

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name Duloxetine Delayed-Release (source: ndc)
Generic Name DULOXETINE HYDROCHLORIDE (source: ndc)
Application Number ANDA203088 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-165-30)
  • 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-165-90)
source: ndc

Packages (2)

60429-165-30 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-165-30) 60429-165-90 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-165-90)

Ingredients (1)

DULOXETINE HYDROCHLORIDE (30 mg/1)

Linked Drug Pages (1)

Duloxetine Delayed-Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a8cefd0-9db7-8cd0-e063-6394a90a5996", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["f535fcd2-a50a-4423-85d9-705fd2d9a470"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-165-30)", "package_ndc": "60429-165-30", "marketing_end_date": "20260228", "marketing_start_date": "20140611"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-165-90)", "package_ndc": "60429-165-90", "marketing_end_date": "20260228", "marketing_start_date": "20140611"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "60429-165_3a8cefd0-9db7-8cd0-e063-6394a90a5996", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60429-165", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20140611"}