zoloft

Generic: sertraline hydrochloride

Labeler: roerig
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name zoloft
Generic Name sertraline hydrochloride
Labeler roerig
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sertraline hydrochloride 50 mg/1

Manufacturer
ROERIG

Identifiers & Regulatory

Product NDC 0049-4900
Product ID 0049-4900_842b5b3f-e0f0-4a16-bb47-2750a605452c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019839
Marketing Start 1992-02-11
Marketing End 2026-06-30

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 00494900
Hyphenated Format 0049-4900

Supplemental Identifiers

RxCUI
208149 208161 212233 312938 312940 312941 861064 861066
UNII
UTI8907Y6X

Packaging Origin

Original Packager
true

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 zoloft (source: ndc)
Generic Name sertraline hydrochloride (source: ndc)
Application Number NDA019839 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (0049-4900-30)
  • 100 BLISTER PACK in 1 CARTON (0049-4900-41) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (2)

0049-4900-30 30 TABLET, FILM COATED in 1 BOTTLE (0049-4900-30) 0049-4900-41 100 BLISTER PACK in 1 CARTON (0049-4900-41) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

sertraline hydrochloride (50 mg/1)

Linked Drug Pages (1)

Zoloft ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "842b5b3f-e0f0-4a16-bb47-2750a605452c", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["208149", "208161", "212233", "312938", "312940", "312941", "861064", "861066"], "spl_set_id": ["fe9e8b7d-61ea-409d-84aa-3ebd79a046b5"], "manufacturer_name": ["ROERIG"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0049-4900-30)", "package_ndc": "0049-4900-30", "marketing_end_date": "20260630", "marketing_start_date": "19920211"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0049-4900-41)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0049-4900-41", "marketing_end_date": "20260630", "marketing_start_date": "19920211"}], "brand_name": "Zoloft", "product_id": "0049-4900_842b5b3f-e0f0-4a16-bb47-2750a605452c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0049-4900", "generic_name": "sertraline hydrochloride", "labeler_name": "ROERIG", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoloft", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "NDA019839", "marketing_category": "NDA", "marketing_end_date": "20260630", "marketing_start_date": "19920211"}