propranolol hydrochloride

Generic: propranolol hydrochloride

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

Drug Facts

Product Profile

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

propranolol hydrochloride 120 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1463
Product ID 70518-1463_4900c8ab-3b55-e02c-e063-6394a90ace9e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078703
Listing Expiration 2027-12-31
Marketing Start 2018-10-04

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181463
Hyphenated Format 70518-1463

Supplemental Identifiers

RxCUI
856460
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 ANDA078703 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1463-0)
source: ndc

Packages (1)

70518-1463-0 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1463-0)

Ingredients (1)

propranolol hydrochloride (120 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": "4900c8ab-3b55-e02c-e063-6394a90ace9e", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856460"], "spl_set_id": ["e0241448-5727-4c68-ae2a-6f41cd962d7c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1463-0)", "package_ndc": "70518-1463-0", "marketing_start_date": "20181004"}], "brand_name": "propranolol hydrochloride", "product_id": "70518-1463_4900c8ab-3b55-e02c-e063-6394a90ace9e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-1463", "generic_name": "propranolol hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "propranolol hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20181004", "listing_expiration_date": "20271231"}