propranolol hydrochloride er

Generic: propranolol hydrochloride

Labeler: ani pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride er
Generic Name propranolol hydrochloride
Labeler ani pharmaceuticals, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

propranolol hydrochloride 160 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 62559-533
Product ID 62559-533_200aecd3-b441-4856-a9fc-6841ada5489c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018553
Listing Expiration 2026-12-31
Marketing Start 2017-12-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62559533
Hyphenated Format 62559-533

Supplemental Identifiers

RxCUI
856460 856481 856535 856569
UPC
0362559531016 0362559533010 0362559532013 0362559530019
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 er (source: ndc)
Generic Name propranolol hydrochloride (source: ndc)
Application Number NDA018553 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62559-533-01)
source: ndc

Packages (1)

62559-533-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62559-533-01)

Ingredients (1)

propranolol hydrochloride (160 mg/1)

Linked Drug Pages (1)

Propranolol Hydrochloride ER ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "200aecd3-b441-4856-a9fc-6841ada5489c", "openfda": {"upc": ["0362559531016", "0362559533010", "0362559532013", "0362559530019"], "unii": ["F8A3652H1V"], "rxcui": ["856460", "856481", "856535", "856569"], "spl_set_id": ["5415904b-90da-48e8-9f9e-f86749aa129c"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62559-533-01)", "package_ndc": "62559-533-01", "marketing_start_date": "20171221"}], "brand_name": "Propranolol Hydrochloride ER", "product_id": "62559-533_200aecd3-b441-4856-a9fc-6841ada5489c", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "62559-533", "generic_name": "propranolol hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "brand_name_suffix": "ER", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "160 mg/1"}], "application_number": "NDA018553", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20171221", "listing_expiration_date": "20261231"}