duloxetine

Generic: duloxetine

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name duloxetine
Generic Name duloxetine
Labeler proficient rx lp
Dosage Form CAPSULE, DELAYED RELEASE PELLETS
Routes
ORAL
Active Ingredients

duloxetine hydrochloride 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-525
Product ID 71205-525_4318dfda-092c-4ade-83c5-581bc968f391
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090776
Listing Expiration 2026-12-31
Marketing Start 2013-12-17

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 71205525
Hyphenated Format 71205-525

Supplemental Identifiers

RxCUI
596926
UPC
0371205525309
UNII
9044SC542W

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

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-30)
  • 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-60)
  • 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-90)
source: ndc

Packages (3)

71205-525-30 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-30) 71205-525-60 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-60) 71205-525-90 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-90)

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 
{"route": ["ORAL"], "spl_id": "4318dfda-092c-4ade-83c5-581bc968f391", "openfda": {"upc": ["0371205525309"], "unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["3dec1805-9a95-462e-8784-303004d500b1"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-30)", "package_ndc": "71205-525-30", "marketing_start_date": "20210122"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-60)", "package_ndc": "71205-525-60", "marketing_start_date": "20210122"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-90)", "package_ndc": "71205-525-90", "marketing_start_date": "20210122"}], "brand_name": "Duloxetine", "product_id": "71205-525_4318dfda-092c-4ade-83c5-581bc968f391", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71205-525", "generic_name": "Duloxetine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090776", "marketing_category": "ANDA", "marketing_start_date": "20131217", "listing_expiration_date": "20261231"}