Package 64380-786-01

Brand: roflumilast

Generic: roflumilast
NDC Package

Package Facts

Identity

Package NDC 64380-786-01
Digits Only 6438078601
Product NDC 64380-786
Product ID 64380-786_9c3f4a61-0aed-418d-b77f-a1864bedee71
Description

30 TABLET in 1 BOTTLE (64380-786-01)

Marketing

Marketing Status
Marketed Since 2022-10-13
Brand roflumilast
Generic roflumilast
Sample Package No

Linked Drug Pages (1)

roflumilast ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9c3f4a61-0aed-418d-b77f-a1864bedee71", "openfda": {}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (64380-786-01)", "package_ndc": "64380-786-01", "marketing_start_date": "20221013"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (64380-786-05)", "package_ndc": "64380-786-05", "marketing_start_date": "20221013"}], "brand_name": "roflumilast", "product_id": "64380-786_9c3f4a61-0aed-418d-b77f-a1864bedee71", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 4 Inhibitor [EPC]", "Phosphodiesterase 4 Inhibitors [MoA]"], "product_ndc": "64380-786", "generic_name": "ROFLUMILAST", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "roflumilast", "active_ingredients": [{"name": "ROFLUMILAST", "strength": "500 ug/1"}], "application_number": "ANDA208247", "marketing_category": "ANDA", "marketing_start_date": "20221013", "listing_expiration_date": "20271231"}