duloxetine
Generic: duloxetine
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
duloxetine
Generic Name
duloxetine
Labeler
bryant ranch prepack
Dosage Form
CAPSULE, DELAYED RELEASE
Routes
Active Ingredients
duloxetine hydrochloride 60 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0402
Product ID
71335-0402_fffa451d-800b-4e92-a01c-5a174e6e32b4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208706
Listing Expiration
2026-12-31
Marketing Start
2017-03-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350402
Hyphenated Format
71335-0402
Supplemental Identifiers
RxCUI
UNII
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
ANDA208706 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
Packaging
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-1)
- 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-2)
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-3)
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-4)
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-5)
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-6)
Packages (6)
71335-0402-1
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-1)
71335-0402-2
28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-2)
71335-0402-3
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-3)
71335-0402-4
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-4)
71335-0402-5
180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-5)
71335-0402-6
120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fffa451d-800b-4e92-a01c-5a174e6e32b4", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["b19ba26f-4711-443e-83cf-5af7bb43a0a0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-1)", "package_ndc": "71335-0402-1", "marketing_start_date": "20180302"}, {"sample": false, "description": "28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-2)", "package_ndc": "71335-0402-2", "marketing_start_date": "20211227"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-3)", "package_ndc": "71335-0402-3", "marketing_start_date": "20180411"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-4)", "package_ndc": "71335-0402-4", "marketing_start_date": "20181030"}, {"sample": false, "description": "180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-5)", "package_ndc": "71335-0402-5", "marketing_start_date": "20181112"}, {"sample": false, "description": "120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-6)", "package_ndc": "71335-0402-6", "marketing_start_date": "20211227"}], "brand_name": "Duloxetine", "product_id": "71335-0402_fffa451d-800b-4e92-a01c-5a174e6e32b4", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71335-0402", "generic_name": "Duloxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20170316", "listing_expiration_date": "20261231"}