propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: ipca laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler ipca laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/1

Manufacturer
Ipca Laboratories Limited

Identifiers & Regulatory

Product NDC 83980-006
Product ID 83980-006_7854dd0a-2a35-4d7f-afe4-210b28966928
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078955
Listing Expiration 2026-12-31
Marketing Start 2024-09-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83980006
Hyphenated Format 83980-006

Supplemental Identifiers

RxCUI
856448 856457 856519 856556 856578
UPC
0383980005013 0383980008014 0383980009011 0383980007017 0383980006010
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 ANDA078955 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (83980-006-01)
  • 500 TABLET in 1 BOTTLE (83980-006-05)
  • 1000 TABLET in 1 BOTTLE (83980-006-10)
  • 30 TABLET in 1 BOTTLE (83980-006-13)
source: ndc

Packages (4)

83980-006-01 100 TABLET in 1 BOTTLE (83980-006-01) 83980-006-05 500 TABLET in 1 BOTTLE (83980-006-05) 83980-006-10 1000 TABLET in 1 BOTTLE (83980-006-10) 83980-006-13 30 TABLET in 1 BOTTLE (83980-006-13)

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": "7854dd0a-2a35-4d7f-afe4-210b28966928", "openfda": {"upc": ["0383980005013", "0383980008014", "0383980009011", "0383980007017", "0383980006010"], "unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519", "856556", "856578"], "spl_set_id": ["9288191e-4d07-4e37-ab66-7b9de9321cf3"], "manufacturer_name": ["Ipca Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (83980-006-01)", "package_ndc": "83980-006-01", "marketing_start_date": "20240919"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (83980-006-05)", "package_ndc": "83980-006-05", "marketing_start_date": "20240919"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (83980-006-10)", "package_ndc": "83980-006-10", "marketing_start_date": "20240919"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (83980-006-13)", "package_ndc": "83980-006-13", "marketing_start_date": "20240919"}], "brand_name": "Propranolol Hydrochloride", "product_id": "83980-006_7854dd0a-2a35-4d7f-afe4-210b28966928", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "83980-006", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Ipca Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078955", "marketing_category": "ANDA", "marketing_start_date": "20240919", "listing_expiration_date": "20261231"}