Package 60687-598-01

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-598-01
Digits Only 6068759801
Product NDC 60687-598
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-598-01) / 1 TABLET in 1 BLISTER PACK (60687-598-11)

Marketing

Marketing Status
Marketed Since 2021-10-19
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2205da94-02fb-4a72-e063-6294a90a396e", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519"], "spl_set_id": ["d027f39e-7648-44c8-a8dc-b26b4cdd81be"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-598-01)  / 1 TABLET in 1 BLISTER PACK (60687-598-11)", "package_ndc": "60687-598-01", "marketing_start_date": "20211019"}], "brand_name": "Propranolol Hydrochloride", "product_id": "60687-598_2205da94-02fb-4a72-e063-6294a90a396e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-598", "generic_name": "Propranolol Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20211019", "listing_expiration_date": "20261231"}