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
71335-2371
Product ID
71335-2371_1bfa8227-93bd-42e2-8051-75ec8b9f8931
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071972
Listing Expiration
2026-12-31
Marketing Start
2021-06-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352371
Hyphenated Format
71335-2371
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
ANDA071972 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 20 TABLET in 1 BOTTLE (71335-2371-1)
- 30 TABLET in 1 BOTTLE (71335-2371-2)
- 100 TABLET in 1 BOTTLE (71335-2371-3)
- 60 TABLET in 1 BOTTLE (71335-2371-4)
- 90 TABLET in 1 BOTTLE (71335-2371-5)
- 180 TABLET in 1 BOTTLE (71335-2371-6)
- 28 TABLET in 1 BOTTLE (71335-2371-7)
- 10 TABLET in 1 BOTTLE (71335-2371-8)
- 120 TABLET in 1 BOTTLE (71335-2371-9)
Packages (9)
71335-2371-1
20 TABLET in 1 BOTTLE (71335-2371-1)
71335-2371-2
30 TABLET in 1 BOTTLE (71335-2371-2)
71335-2371-3
100 TABLET in 1 BOTTLE (71335-2371-3)
71335-2371-4
60 TABLET in 1 BOTTLE (71335-2371-4)
71335-2371-5
90 TABLET in 1 BOTTLE (71335-2371-5)
71335-2371-6
180 TABLET in 1 BOTTLE (71335-2371-6)
71335-2371-7
28 TABLET in 1 BOTTLE (71335-2371-7)
71335-2371-8
10 TABLET in 1 BOTTLE (71335-2371-8)
71335-2371-9
120 TABLET in 1 BOTTLE (71335-2371-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1bfa8227-93bd-42e2-8051-75ec8b9f8931", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["1d79ba59-6346-46c0-8e63-470e2069238e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-2371-1)", "package_ndc": "71335-2371-1", "marketing_start_date": "20240523"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2371-2)", "package_ndc": "71335-2371-2", "marketing_start_date": "20240523"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2371-3)", "package_ndc": "71335-2371-3", "marketing_start_date": "20240523"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2371-4)", "package_ndc": "71335-2371-4", "marketing_start_date": "20240523"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2371-5)", "package_ndc": "71335-2371-5", "marketing_start_date": "20240523"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-2371-6)", "package_ndc": "71335-2371-6", "marketing_start_date": "20240523"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2371-7)", "package_ndc": "71335-2371-7", "marketing_start_date": "20240523"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2371-8)", "package_ndc": "71335-2371-8", "marketing_start_date": "20240523"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2371-9)", "package_ndc": "71335-2371-9", "marketing_start_date": "20240523"}], "brand_name": "Propranolol Hydrochloride", "product_id": "71335-2371_1bfa8227-93bd-42e2-8051-75ec8b9f8931", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2371", "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": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20261231"}