duloxetine delayed-release

Generic: duloxetine hydrochloride

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

Drug Facts

Product Profile

Brand Name duloxetine delayed-release
Generic Name duloxetine hydrochloride
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 63187-720
Product ID 63187-720_1f36294a-3092-46a3-9d23-9d0c1a3e6254
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203088
Listing Expiration 2026-12-31
Marketing Start 2014-06-11

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 63187720
Hyphenated Format 63187-720

Supplemental Identifiers

RxCUI
596926
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 delayed-release (source: ndc)
Generic Name duloxetine hydrochloride (source: ndc)
Application Number ANDA203088 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-30)
  • 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-60)
  • 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-90)
source: ndc

Packages (3)

63187-720-30 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-30) 63187-720-60 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-60) 63187-720-90 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-90)

Ingredients (1)

duloxetine hydrochloride (20 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": "1f36294a-3092-46a3-9d23-9d0c1a3e6254", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["407b62b9-5b32-4bac-a2b0-7df499279248"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-30)", "package_ndc": "63187-720-30", "marketing_start_date": "20160601"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-60)", "package_ndc": "63187-720-60", "marketing_start_date": "20160601"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-90)", "package_ndc": "63187-720-90", "marketing_start_date": "20160601"}], "brand_name": "DULOXETINE DELAYED-RELEASE", "product_id": "63187-720_1f36294a-3092-46a3-9d23-9d0c1a3e6254", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63187-720", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DULOXETINE", "brand_name_suffix": "DELAYED-RELEASE", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}