propranolol hydrochloride

Generic: propranolol hydrochloride

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

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

propranolol hydrochloride 1 mg/mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9872
Product ID 0143-9872_4432e36f-bed0-4e42-87aa-1330d1725963
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077760
Listing Expiration 2027-12-31
Marketing Start 2008-01-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439872
Hyphenated Format 0143-9872

Supplemental Identifiers

RxCUI
856443
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 ANDA077760 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (0143-9872-10) / 1 mL in 1 VIAL (0143-9872-01)
source: ndc

Packages (1)

Ingredients (1)

propranolol hydrochloride (1 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "4432e36f-bed0-4e42-87aa-1330d1725963", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856443"], "spl_set_id": ["91f2ff1d-68d8-4e83-a2db-618f0410ead7"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9872-10)  / 1 mL in 1 VIAL (0143-9872-01)", "package_ndc": "0143-9872-10", "marketing_start_date": "20080131"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0143-9872_4432e36f-bed0-4e42-87aa-1330d1725963", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0143-9872", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA077760", "marketing_category": "ANDA", "marketing_start_date": "20080131", "listing_expiration_date": "20271231"}