propranolol hydrochloride
Generic: propranolol hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
propranolol hydrochloride
Generic Name
propranolol hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
propranolol hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-2277
Product ID
63629-2277_5903fa58-2cbc-4783-99e5-ab212c4e8388
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA070221
Listing Expiration
2026-12-31
Marketing Start
2010-06-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636292277
Hyphenated Format
63629-2277
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
propranolol hydrochloride (source: ndc)
Generic Name
propranolol hydrochloride (source: ndc)
Application Number
ANDA070221 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 1000 TABLET in 1 BOTTLE (63629-2277-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5903fa58-2cbc-4783-99e5-ab212c4e8388", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["062a1734-00d1-4871-8e7e-450b0ff5864c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-2277-1)", "package_ndc": "63629-2277-1", "marketing_start_date": "20100621"}], "brand_name": "Propranolol Hydrochloride", "product_id": "63629-2277_5903fa58-2cbc-4783-99e5-ab212c4e8388", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-2277", "generic_name": "propranolol hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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": "20100621", "listing_expiration_date": "20261231"}