Package 66267-261-90

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 66267-261-90
Digits Only 6626726190
Product NDC 66267-261
Product ID 66267-261_1fa6afe6-d920-02d3-e063-6394a90a41c7
Description

90 TABLET in 1 BOTTLE (66267-261-90)

Marketing

Marketing Status
Marketed Since 2019-09-17
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": "1fa6afe6-d920-02d3-e063-6394a90a41c7", "openfda": {"upc": ["0366267261906"], "unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["92c4bd8f-d0e6-d11a-e053-2995a90a635d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (66267-261-90)", "package_ndc": "66267-261-90", "marketing_start_date": "20190917"}], "brand_name": "Propranolol Hydrochloride", "product_id": "66267-261_1fa6afe6-d920-02d3-e063-6394a90a41c7", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "66267-261", "generic_name": "propranolol hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070217", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}