Package 43063-840-30
Brand: diazepam
Generic: diazepamPackage Facts
Identity
Package NDC
43063-840-30
Digits Only
4306384030
Product NDC
43063-840
Description
30 TABLET in 1 BOTTLE, PLASTIC (43063-840-30)
Marketing
Marketing Status
Brand
diazepam
Generic
diazepam
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "415be6c2-6829-8f06-e063-6394a90ae555", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0343063840306"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197590"], "spl_set_id": ["1ad84940-40f7-457a-8ffa-53e1a7bfee16"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-840-30)", "package_ndc": "43063-840-30", "marketing_start_date": "20180322"}], "brand_name": "Diazepam", "product_id": "43063-840_415be6c2-6829-8f06-e063-6394a90ae555", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "43063-840", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "2 mg/1"}], "application_number": "ANDA071307", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}