Package 51655-302-26

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-302-26
Digits Only 5165530226
Product NDC 51655-302
Product ID 51655-302_48eadbc7-2351-2bb6-e063-6294a90a067d
Description

90 TABLET in 1 BOTTLE, PLASTIC (51655-302-26)

Marketing

Marketing Status
Marketed Since 2020-05-19
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Propranolol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48eadbc7-2351-2bb6-e063-6294a90a067d", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["f2b8b894-d887-c4ee-e053-2995a90a0c0b"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-302-26)", "package_ndc": "51655-302-26", "marketing_start_date": "20200519"}], "brand_name": "Propranolol Hydrochloride", "product_id": "51655-302_48eadbc7-2351-2bb6-e063-6294a90a067d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51655-302", "generic_name": "propranolol hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA070221", "marketing_category": "ANDA", "marketing_start_date": "20200519", "listing_expiration_date": "20271231"}