propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler actavis pharma, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

propranolol hydrochloride 160 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0228-2781
Product ID 0228-2781_1f70f68b-1314-4c20-872e-993e0f33fb43
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078494
Listing Expiration 2026-12-31
Marketing Start 2007-08-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02282781
Hyphenated Format 0228-2781

Supplemental Identifiers

RxCUI
856460 856481 856535 856569
UPC
0302282780114
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 ANDA078494 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-2781-11)
source: ndc

Packages (1)

0228-2781-11 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-2781-11)

Ingredients (1)

propranolol hydrochloride (160 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": "1f70f68b-1314-4c20-872e-993e0f33fb43", "openfda": {"upc": ["0302282780114"], "unii": ["F8A3652H1V"], "rxcui": ["856460", "856481", "856535", "856569"], "spl_set_id": ["a4edba76-29b8-41fb-bf0b-d4633abba003"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-2781-11)", "package_ndc": "0228-2781-11", "marketing_start_date": "20070810"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0228-2781_1f70f68b-1314-4c20-872e-993e0f33fb43", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0228-2781", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "160 mg/1"}], "application_number": "ANDA078494", "marketing_category": "ANDA", "marketing_start_date": "20070810", "listing_expiration_date": "20261231"}