Package 43063-541-45
Brand: benzphetamine hydrochloride
Generic: benzphetamine hydrochloridePackage Facts
Identity
Package NDC
43063-541-45
Digits Only
4306354145
Product NDC
43063-541
Description
45 TABLET in 1 BOTTLE, PLASTIC (43063-541-45)
Marketing
Marketing Status
Brand
benzphetamine hydrochloride
Generic
benzphetamine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41393fbe-29e5-dd10-e063-6394a90a5a13", "openfda": {"upc": ["0343063541609"], "unii": ["43DWT87QT7"], "rxcui": ["904368"], "spl_set_id": ["2b7014af-0cc9-4199-90f2-ec07ac02f8cf"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-541-14)", "package_ndc": "43063-541-14", "marketing_start_date": "20141022"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-541-30)", "package_ndc": "43063-541-30", "marketing_start_date": "20141022"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE, PLASTIC (43063-541-45)", "package_ndc": "43063-541-45", "marketing_start_date": "20141022"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-541-60)", "package_ndc": "43063-541-60", "marketing_start_date": "20141022"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-541-90)", "package_ndc": "43063-541-90", "marketing_start_date": "20141022"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (43063-541-98)", "package_ndc": "43063-541-98", "marketing_start_date": "20100721"}], "brand_name": "BENZPHETAMINE HYDROCHLORIDE", "product_id": "43063-541_41393fbe-29e5-dd10-e063-6394a90a5a13", "dosage_form": "TABLET", "pharm_class": ["Appetite Suppression [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic Amine Anorectic [EPC]"], "product_ndc": "43063-541", "dea_schedule": "CIII", "generic_name": "benzphetamine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BENZPHETAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "BENZPHETAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA090968", "marketing_category": "ANDA", "marketing_start_date": "20100721", "listing_expiration_date": "20261231"}