labetalol hcl in sodium chloride
Generic: labetalol hydrochloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
labetalol hcl in sodium chloride
Generic Name
labetalol hydrochloride
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
labetalol hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9363
Product ID
0143-9363_d0e3d92d-d96e-4d5e-98ca-3d18a4bc82d8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA213330
Listing Expiration
2026-12-31
Marketing Start
2020-11-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439363
Hyphenated Format
0143-9363
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
labetalol hcl in sodium chloride (source: ndc)
Generic Name
labetalol hydrochloride (source: ndc)
Application Number
NDA213330 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 BAG in 1 BOX (0143-9363-10) / 100 mL in 1 BAG (0143-9363-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d0e3d92d-d96e-4d5e-98ca-3d18a4bc82d8", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["2477889", "2479564", "2479566", "2479567"], "spl_set_id": ["99a715a0-4579-410c-b102-7ef6fab8db55"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 BOX (0143-9363-10) / 100 mL in 1 BAG (0143-9363-01)", "package_ndc": "0143-9363-10", "marketing_start_date": "20201109"}], "brand_name": "Labetalol HCl in Sodium Chloride", "product_id": "0143-9363_d0e3d92d-d96e-4d5e-98ca-3d18a4bc82d8", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0143-9363", "generic_name": "LABETALOL HYDROCHLORIDE", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol HCl in Sodium Chloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "NDA213330", "marketing_category": "NDA", "marketing_start_date": "20201109", "listing_expiration_date": "20261231"}