labetalol hcl in dextrose
Generic: labetalol hydrochloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
labetalol hcl in dextrose
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
0143-9366
Product ID
0143-9366_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
01439366
Hyphenated Format
0143-9366
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 dextrose (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 (0143-9366-10) / 200 mL in 1 BAG (0143-9366-01)
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 (0143-9366-10) / 200 mL in 1 BAG (0143-9366-01)", "package_ndc": "0143-9366-10", "marketing_start_date": "20201109"}], "brand_name": "Labetalol HCl in Dextrose", "product_id": "0143-9366_d0e3d92d-d96e-4d5e-98ca-3d18a4bc82d8", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0143-9366", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol HCl in Dextrose", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "NDA213330", "marketing_category": "NDA", "marketing_start_date": "20201109", "listing_expiration_date": "20261231"}