Package 60687-641-21

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 60687-641-21
Digits Only 6068764121
Product NDC 60687-641
Product ID 60687-641_35420d8c-7a05-0220-e063-6394a90a1c25
Description

30 BLISTER PACK in 1 CARTON (60687-641-21) / 1 TABLET in 1 BLISTER PACK (60687-641-11)

Marketing

Marketing Status
Marketed Since 2022-09-07
Brand nebivolol
Generic nebivolol
Sample Package No

Linked Drug Pages (1)

Nebivolol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35420d8c-7a05-0220-e063-6394a90a1c25", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612"], "spl_set_id": ["5418f2b2-3e23-4e7a-b4df-36a1515c9a12"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-641-21)  / 1 TABLET in 1 BLISTER PACK (60687-641-11)", "package_ndc": "60687-641-21", "marketing_start_date": "20220907"}], "brand_name": "Nebivolol", "product_id": "60687-641_35420d8c-7a05-0220-e063-6394a90a1c25", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-641", "generic_name": "Nebivolol", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203828", "marketing_category": "ANDA", "marketing_start_date": "20220907", "listing_expiration_date": "20261231"}