sertraline hydrochloride

Generic: sertraline hydrochloride

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sertraline hydrochloride
Generic Name sertraline hydrochloride
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sertraline hydrochloride 50 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8603
Product ID 0615-8603_339cfb58-17b5-460a-a7bb-fd5334fbc148
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077670
Listing Expiration 2027-12-31
Marketing Start 2007-02-06

Pharmacologic Class

Classes
cytochrome p450 2d6 inhibitors [moa] serotonin reuptake inhibitor [epc] serotonin uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06158603
Hyphenated Format 0615-8603

Supplemental Identifiers

RxCUI
312938 312940 312941
UNII
UTI8907Y6X

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 sertraline hydrochloride (source: ndc)
Generic Name sertraline hydrochloride (source: ndc)
Application Number ANDA077670 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8603-05)
  • 28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8603-28)
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8603-39)
source: ndc

Packages (3)

0615-8603-05 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8603-05) 0615-8603-28 28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8603-28) 0615-8603-39 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8603-39)

Ingredients (1)

sertraline hydrochloride (50 mg/1)

Linked Drug Pages (1)

Sertraline Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "339cfb58-17b5-460a-a7bb-fd5334fbc148", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938", "312940", "312941"], "spl_set_id": ["fd92c8d3-17ec-477c-bc25-e5239c8606ac"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8603-05)", "package_ndc": "0615-8603-05", "marketing_start_date": "20251119"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8603-28)", "package_ndc": "0615-8603-28", "marketing_start_date": "20251119"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8603-39)", "package_ndc": "0615-8603-39", "marketing_start_date": "20251119"}], "brand_name": "Sertraline Hydrochloride", "product_id": "0615-8603_339cfb58-17b5-460a-a7bb-fd5334fbc148", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0615-8603", "generic_name": "Sertraline Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA077670", "marketing_category": "ANDA", "marketing_start_date": "20070206", "listing_expiration_date": "20271231"}