Package 47335-929-75

Brand: temozolomide

Generic: temozolomide
NDC Package

Package Facts

Identity

Package NDC 47335-929-75
Digits Only 4733592975
Product NDC 47335-929
Description

20 BLISTER PACK in 1 CARTON (47335-929-75) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-02-13
Brand temozolomide
Generic temozolomide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7c774570-443b-40da-8038-7cb550f92048", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["YF1K15M17Y"], "rxcui": ["313209", "313210", "313211", "317160", "700883", "700885"], "spl_set_id": ["c1e05c21-a411-4493-80de-ede373632475"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (47335-929-21)  / 14 CAPSULE in 1 BOTTLE", "package_ndc": "47335-929-21", "marketing_start_date": "20140213"}, {"sample": false, "description": "15 BLISTER PACK in 1 CARTON (47335-929-72)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "47335-929-72", "marketing_start_date": "20140213"}, {"sample": false, "description": "5 BLISTER PACK in 1 CARTON (47335-929-74)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "47335-929-74", "marketing_start_date": "20140213"}, {"sample": false, "description": "20 BLISTER PACK in 1 CARTON (47335-929-75)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "47335-929-75", "marketing_start_date": "20140213"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (47335-929-80)  / 5 CAPSULE in 1 BOTTLE", "package_ndc": "47335-929-80", "marketing_start_date": "20140213"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (47335-929-87)  / 20 CAPSULE in 1 BOTTLE", "package_ndc": "47335-929-87", "marketing_start_date": "20140213"}], "brand_name": "Temozolomide", "product_id": "47335-929_7c774570-443b-40da-8038-7cb550f92048", "dosage_form": "CAPSULE", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "47335-929", "generic_name": "Temozolomide", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Temozolomide", "active_ingredients": [{"name": "TEMOZOLOMIDE", "strength": "140 mg/1"}], "application_number": "ANDA201742", "marketing_category": "ANDA", "marketing_start_date": "20140213", "listing_expiration_date": "20261231"}