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 30 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-702
Product ID 63187-702_baacd94b-8cee-45ad-9bb4-cd12a8cfbd58
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 63187702
Hyphenated Format 63187-702

Supplemental Identifiers

RxCUI
596930
UPC
0363187702304
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
  • 30 mg/1
source: ndc
Packaging
  • 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-30)
  • 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-60)
  • 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-90)
source: ndc

Packages (3)

63187-702-30 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-30) 63187-702-60 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-60) 63187-702-90 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-90)

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": "baacd94b-8cee-45ad-9bb4-cd12a8cfbd58", "openfda": {"upc": ["0363187702304"], "unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["41c86c02-68c0-4db5-af1a-941b0d2ffe11"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-30)", "package_ndc": "63187-702-30", "marketing_start_date": "20160502"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-60)", "package_ndc": "63187-702-60", "marketing_start_date": "20160502"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-90)", "package_ndc": "63187-702-90", "marketing_start_date": "20160502"}], "brand_name": "DULOXETINE DELAYED-RELEASE", "product_id": "63187-702_baacd94b-8cee-45ad-9bb4-cd12a8cfbd58", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "63187-702", "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": "30 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}