propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: mylan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler mylan pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 0378-0183
Product ID 0378-0183_00b5d450-69b9-45c8-812f-04444bde36b0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070213
Listing Expiration 2027-12-31
Marketing Start 1985-11-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03780183
Hyphenated Format 0378-0183

Supplemental Identifiers

UPC
0303780187016 0303780185012 0303780184015 0303780182011 0303780183018
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 ANDA070213 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (0378-0183-01)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (0378-0183-10)
source: ndc

Packages (2)

0378-0183-01 100 TABLET in 1 BOTTLE, PLASTIC (0378-0183-01) 0378-0183-10 1000 TABLET in 1 BOTTLE, PLASTIC (0378-0183-10)

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": "00b5d450-69b9-45c8-812f-04444bde36b0", "openfda": {"upc": ["0303780187016", "0303780185012", "0303780184015", "0303780182011", "0303780183018"], "unii": ["F8A3652H1V"], "spl_set_id": ["b94dcec7-7633-4a33-9cea-48161adeaf93"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0378-0183-01)", "package_ndc": "0378-0183-01", "marketing_start_date": "19851119"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0378-0183-10)", "package_ndc": "0378-0183-10", "marketing_start_date": "19851119"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0378-0183_00b5d450-69b9-45c8-812f-04444bde36b0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0378-0183", "generic_name": "propranolol hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA070213", "marketing_category": "ANDA", "marketing_start_date": "19851119", "listing_expiration_date": "20271231"}