Package 0049-4900-41

Brand: zoloft

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0049-4900-41
Digits Only 0049490041
Product NDC 0049-4900
Description

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

Marketing

Marketing Status
Discontinued 2026-06-30
Brand zoloft
Generic sertraline hydrochloride
Sample Package No

Linked Drug Pages (1)

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"}