cymbalta

Generic: duloxetine hydrochloride

Labeler: eli lilly and company
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name cymbalta
Generic Name duloxetine hydrochloride
Labeler eli lilly and company
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

duloxetine hydrochloride 30 mg/1

Manufacturer
Eli Lilly and Company

Identifiers & Regulatory

Product NDC 0002-3240
Product ID 0002-3240_aa5061b1-f237-425a-9d05-575c333dfd37
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021427
Marketing Start 2004-08-24
Marketing End 2026-10-02

Pharmacologic Class

Classes
norepinephrine uptake inhibitors [moa] serotonin uptake inhibitors [moa] serotonin and norepinephrine reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00023240
Hyphenated Format 0002-3240

Supplemental Identifiers

RxCUI
596926 596928 596930 596932 596934 615186
UPC
0300023270306 0300023240309 0300023235602
UNII
9044SC542W

Packaging Origin

Original Packager
true

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 cymbalta (source: ndc)
Generic Name duloxetine hydrochloride (source: ndc)
Application Number NDA021427 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3240-30)
  • 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3240-90)
source: ndc

Packages (2)

0002-3240-30 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3240-30) 0002-3240-90 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3240-90)

Ingredients (1)

duloxetine hydrochloride (30 mg/1)

Linked Drug Pages (1)

Cymbalta ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "aa5061b1-f237-425a-9d05-575c333dfd37", "openfda": {"upc": ["0300023270306", "0300023240309", "0300023235602"], "unii": ["9044SC542W"], "rxcui": ["596926", "596928", "596930", "596932", "596934", "615186"], "spl_set_id": ["2f7d4d67-10c1-4bf4-a7f2-c185fbad64ba"], "manufacturer_name": ["Eli Lilly and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3240-30)", "package_ndc": "0002-3240-30", "marketing_end_date": "20260417", "marketing_start_date": "20040824"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3240-90)", "package_ndc": "0002-3240-90", "marketing_end_date": "20260417", "marketing_start_date": "20040824"}], "brand_name": "Cymbalta", "product_id": "0002-3240_aa5061b1-f237-425a-9d05-575c333dfd37", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0002-3240", "generic_name": "Duloxetine hydrochloride", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cymbalta", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "NDA021427", "marketing_category": "NDA", "marketing_end_date": "20261002", "marketing_start_date": "20040824"}