propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler asclemed usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 40 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-385
Product ID 76420-385_366b6b94-8ad2-8ec9-e063-6394a90a813b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070322
Listing Expiration 2026-12-31
Marketing Start 2019-10-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420385
Hyphenated Format 76420-385

Supplemental Identifiers

RxCUI
856448 856457 856519 856556 856578
UNII
F8A3652H1V

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 ANDA070322 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (76420-385-00)
  • 100 TABLET in 1 BOTTLE (76420-385-01)
  • 20 TABLET in 1 BOTTLE (76420-385-20)
  • 30 TABLET in 1 BOTTLE (76420-385-30)
  • 60 TABLET in 1 BOTTLE (76420-385-60)
  • 90 TABLET in 1 BOTTLE (76420-385-90)
source: ndc

Packages (6)

76420-385-00 1000 TABLET in 1 BOTTLE (76420-385-00) 76420-385-01 100 TABLET in 1 BOTTLE (76420-385-01) 76420-385-20 20 TABLET in 1 BOTTLE (76420-385-20) 76420-385-30 30 TABLET in 1 BOTTLE (76420-385-30) 76420-385-60 60 TABLET in 1 BOTTLE (76420-385-60) 76420-385-90 90 TABLET in 1 BOTTLE (76420-385-90)

Ingredients (1)

propranolol hydrochloride (40 mg/1)

Linked Drug Pages (1)

Propranolol Hydrochloride, Propranolol hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "366b6b94-8ad2-8ec9-e063-6394a90a813b", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519", "856556", "856578"], "spl_set_id": ["d08dbabc-8ca4-426e-a9fd-e7914a27883c"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (76420-385-00)", "package_ndc": "76420-385-00", "marketing_start_date": "20250331"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-385-01)", "package_ndc": "76420-385-01", "marketing_start_date": "20250331"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (76420-385-20)", "package_ndc": "76420-385-20", "marketing_start_date": "20250331"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-385-30)", "package_ndc": "76420-385-30", "marketing_start_date": "20250331"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-385-60)", "package_ndc": "76420-385-60", "marketing_start_date": "20250331"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-385-90)", "package_ndc": "76420-385-90", "marketing_start_date": "20250331"}], "brand_name": "Propranolol Hydrochloride", "product_id": "76420-385_366b6b94-8ad2-8ec9-e063-6394a90a813b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "76420-385", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20191031", "listing_expiration_date": "20261231"}