Package 43598-036-01
Brand: fluphenazine hydrochloride
Generic: fluphenazine hydrochloridePackage Facts
Identity
Package NDC
43598-036-01
Digits Only
4359803601
Product NDC
43598-036
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43598-036-01)
Marketing
Marketing Status
Brand
fluphenazine hydrochloride
Generic
fluphenazine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "95c5a977-cf1e-488a-8eff-c5fabc4b73c3", "openfda": {"upc": ["0343598037011", "0343598036014", "0343598034010", "0343598035017"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["98aeddfd-4f24-4d1a-820d-d0abc1733794"], "manufacturer_name": ["Dr. Reddys Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43598-036-01)", "package_ndc": "43598-036-01", "marketing_start_date": "20210215"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "43598-036_95c5a977-cf1e-488a-8eff-c5fabc4b73c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "43598-036", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Dr. Reddys Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA214534", "marketing_category": "ANDA", "marketing_start_date": "20210215", "listing_expiration_date": "20261231"}