Package 68071-4922-6

Brand: diazepam

Generic: diazepam
NDC Package

Package Facts

Identity

Package NDC 68071-4922-6
Digits Only 6807149226
Product NDC 68071-4922
Description

6 TABLET in 1 BOTTLE (68071-4922-6)

Marketing

Marketing Status
Marketed Since 2019-06-13
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": "1ae25c30-4082-3b15-e063-6394a90af42f", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0368071492262"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197591"], "spl_set_id": ["8b3cc5c9-91bd-7467-e053-2a95a90a44b8"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-4922-1)", "package_ndc": "68071-4922-1", "marketing_start_date": "20190613"}, {"sample": false, "description": "8 TABLET in 1 BOTTLE (68071-4922-4)", "package_ndc": "68071-4922-4", "marketing_start_date": "20190613"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-4922-6)", "package_ndc": "68071-4922-6", "marketing_start_date": "20190613"}], "brand_name": "Diazepam", "product_id": "68071-4922_1ae25c30-4082-3b15-e063-6394a90af42f", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "68071-4922", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "NuCare 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"}