Fluoxetine

Generic: Fluoxetine Hydrochloride

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Fluoxetine
Generic Name Fluoxetine Hydrochloride
Labeler REMEDYREPACK INC.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

FLUOXETINE HYDROCHLORIDE 20 mg/1

Identifiers & Regulatory

Product NDC 70518-1359
Product ID 70518-1359_48e928c8-ff32-4ff8-e063-6394a90ae57f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078619
Listing Expiration 2027-12-31
Marketing Start 2018-08-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181359
Hyphenated Format 70518-1359

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 Fluoxetine (source: ndc)
Generic Name Fluoxetine Hydrochloride (source: ndc)
Application Number ANDA078619 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BLISTER PACK (70518-1359-2)
source: ndc

Packages (1)

70518-1359-2 30 CAPSULE in 1 BLISTER PACK (70518-1359-2)

Ingredients (1)

FLUOXETINE HYDROCHLORIDE (20 mg/1)

Linked Drug Pages (1)

Fluoxetine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48e928c8-ff32-4ff8-e063-6394a90ae57f", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["aa463a85-3c2e-4465-a548-d2cb590e5db9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-1359-2)", "package_ndc": "70518-1359-2", "marketing_start_date": "20200502"}], "brand_name": "Fluoxetine", "product_id": "70518-1359_48e928c8-ff32-4ff8-e063-6394a90ae57f", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-1359", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20180809", "listing_expiration_date": "20271231"}