propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler proficient rx lp
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

propranolol hydrochloride 60 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-760
Product ID 71205-760_968353ed-eb79-4f96-9569-3efb220fc388
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 71205760
Hyphenated Format 71205-760

Supplemental Identifiers

RxCUI
856535
UPC
0371205760304
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 ANDA078494 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-30)
  • 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-60)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-90)
source: ndc

Packages (3)

71205-760-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-30) 71205-760-60 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-60) 71205-760-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-90)

Ingredients (1)

propranolol hydrochloride (60 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": "968353ed-eb79-4f96-9569-3efb220fc388", "openfda": {"upc": ["0371205760304"], "unii": ["F8A3652H1V"], "rxcui": ["856535"], "spl_set_id": ["968353ed-eb79-4f96-9569-3efb220fc388"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-30)", "package_ndc": "71205-760-30", "marketing_start_date": "20230209"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-60)", "package_ndc": "71205-760-60", "marketing_start_date": "20230209"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-760-90)", "package_ndc": "71205-760-90", "marketing_start_date": "20230209"}], "brand_name": "Propranolol Hydrochloride", "product_id": "71205-760_968353ed-eb79-4f96-9569-3efb220fc388", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71205-760", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA078494", "marketing_category": "ANDA", "marketing_start_date": "20070810", "listing_expiration_date": "20261231"}