Package 43063-970-06

Brand: diazepam

Generic: diazepam
NDC Package

Package Facts

Identity

Package NDC 43063-970-06
Digits Only 4306397006
Product NDC 43063-970
Description

6 TABLET in 1 BOTTLE, PLASTIC (43063-970-06)

Marketing

Marketing Status
Marketed Since 2019-05-13
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": "415f6daf-09f1-78a5-e063-6294a90a9553", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0343063970300"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197591"], "spl_set_id": ["2483426d-3782-432a-8b8d-86c06ef0de4a"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE, PLASTIC (43063-970-04)", "package_ndc": "43063-970-04", "marketing_start_date": "20190731"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (43063-970-06)", "package_ndc": "43063-970-06", "marketing_start_date": "20190513"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (43063-970-10)", "package_ndc": "43063-970-10", "marketing_start_date": "20200805"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (43063-970-15)", "package_ndc": "43063-970-15", "marketing_start_date": "20191204"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (43063-970-21)", "package_ndc": "43063-970-21", "marketing_start_date": "20190507"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-970-30)", "package_ndc": "43063-970-30", "marketing_start_date": "20190501"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-970-60)", "package_ndc": "43063-970-60", "marketing_start_date": "20191126"}], "brand_name": "Diazepam", "product_id": "43063-970_415f6daf-09f1-78a5-e063-6294a90a9553", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "43063-970", "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": "5 mg/1"}], "application_number": "ANDA071321", "marketing_category": "ANDA", "marketing_start_date": "19861210", "listing_expiration_date": "20261231"}