0228-2890

Generic: duloxetine

Labeler: actavis pharma, inc.
NDC Directory DRUG FOR FURTHER PROCESSING DRUG FOR FURTHER PROCESSING Active

Drug Facts

Product Profile

Brand Name
Generic Name duloxetine
Labeler actavis pharma, inc.
Dosage Form CAPSULE, DELAYED RELEASE PELLETS
Active Ingredients

duloxetine hydrochloride 20 mg/1

Identifiers & Regulatory

Product NDC 0228-2890
Product ID 0228-2890_0a2a092f-eef2-480e-840c-a530a1ea2bdb
Product Type DRUG FOR FURTHER PROCESSING
Marketing Category DRUG FOR FURTHER PROCESSING
Listing Expiration 2026-12-31
Marketing Start 2024-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02282890
Hyphenated Format 0228-2890

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 (source: label)
Generic Name duloxetine (source: ndc)
Application Number ANDA090776 (source: label)
Routes
oral
source: label

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 26792 CAPSULE, DELAYED RELEASE PELLETS in 1 CONTAINER (0228-2890-00)
source: ndc

Packages (1)

0228-2890-00 26792 CAPSULE, DELAYED RELEASE PELLETS in 1 CONTAINER (0228-2890-00)

Ingredients (1)

duloxetine hydrochloride (20 mg/1)

Linked Drug Pages (1)

Duloxetine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "0a2a092f-eef2-480e-840c-a530a1ea2bdb", "openfda": {}, "finished": false, "packaging": [{"description": "26792 CAPSULE, DELAYED RELEASE PELLETS in 1 CONTAINER (0228-2890-00)", "package_ndc": "0228-2890-00", "marketing_start_date": "01-FEB-24"}], "product_id": "0228-2890_0a2a092f-eef2-480e-840c-a530a1ea2bdb", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "product_ndc": "0228-2890", "generic_name": "Duloxetine", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20240201", "listing_expiration_date": "20261231"}