sertraline hydrochloride

Generic: sertraline hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sertraline hydrochloride
Generic Name sertraline hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sertraline hydrochloride 50 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2812
Product ID 70518-2812_4aa3e16a-2372-5ed2-e063-6294a90ad6d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077206
Listing Expiration 2027-12-31
Marketing Start 2020-07-10

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 705182812
Hyphenated Format 70518-2812

Supplemental Identifiers

RxCUI
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 ANDA077206 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-5)
source: ndc

Packages (3)

70518-2812-1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-1) 70518-2812-2 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-2) 70518-2812-5 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-5)

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": "4aa3e16a-2372-5ed2-e063-6294a90ad6d9", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["91e24d17-ff0a-449c-9472-b9df74c98456"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-1)", "package_ndc": "70518-2812-1", "marketing_start_date": "20200815"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-2)", "package_ndc": "70518-2812-2", "marketing_start_date": "20201102"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-5)", "package_ndc": "70518-2812-5", "marketing_start_date": "20250219"}], "brand_name": "Sertraline Hydrochloride", "product_id": "70518-2812_4aa3e16a-2372-5ed2-e063-6294a90ad6d9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-2812", "generic_name": "Sertraline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20200710", "listing_expiration_date": "20271231"}