propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: lifestar pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler lifestar pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/1

Manufacturer
Lifestar Pharma LLC

Identifiers & Regulatory

Product NDC 70756-095
Product ID 70756-095_f1ed91cc-9651-41e9-bc21-855bdf78e5fc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216663
Listing Expiration 2027-12-31
Marketing Start 2026-01-27

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70756095
Hyphenated Format 70756-095

Supplemental Identifiers

RxCUI
856448 856457 856519 856556 856578
UPC
0370756296119 0370756296126 0370756095118
UNII
F8A3652H1V

Packaging Origin

Original Packager
true

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 ANDA216663 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70756-095-11)
  • 1000 TABLET in 1 BOTTLE (70756-095-12)
source: ndc

Packages (2)

70756-095-11 100 TABLET in 1 BOTTLE (70756-095-11) 70756-095-12 1000 TABLET in 1 BOTTLE (70756-095-12)

Ingredients (1)

propranolol hydrochloride (20 mg/1)

Linked Drug Pages (1)

Propranolol hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f1ed91cc-9651-41e9-bc21-855bdf78e5fc", "openfda": {"upc": ["0370756296119", "0370756296126", "0370756095118"], "unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519", "856556", "856578"], "spl_set_id": ["25f9b9a3-7b0b-48d2-a458-c613bedc7cab"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70756-095-11)", "package_ndc": "70756-095-11", "marketing_start_date": "20260127"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70756-095-12)", "package_ndc": "70756-095-12", "marketing_start_date": "20260127"}], "brand_name": "Propranolol hydrochloride", "product_id": "70756-095_f1ed91cc-9651-41e9-bc21-855bdf78e5fc", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70756-095", "generic_name": "Propranolol hydrochloride", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA216663", "marketing_category": "ANDA", "marketing_start_date": "20260127", "listing_expiration_date": "20271231"}