Labetalol Hydrochloride

Product NDC
0143-9622
11-digit product format
001439622
Labeler code
0143
Product ID
0143-9622_069ca72e-bf5a-440a-9169-19f1ac7f7126
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Labetalol Hydrochloride
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
Hikma Pharmaceuticals USA Inc.
Application
ANDA075303
Marketing category
ANDA
Marketing start
1999-11-29
Substance
LABETALOL HYDROCHLORIDE
Active strength
5 mg/mL
Pharmacologic classes
Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Labetalol Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LABETALOL HYDROCHLORIDE5 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1GEV3BAW9J
Rxcui896771

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
cb89b86a-369e-4204-8910-ae797c503af3Product name120230706
baf61d8c-dcd3-e95d-db84-9bb0d0a2b77fProduct name220220311
759f1c41-9262-4238-8cee-33988631aaf4Product name520220217
3b2edbb4-6acf-4674-b1d9-22addd3dad21Product name120210527
d4880ace-a516-8c47-8dfd-73a4ba5887d7Product name220180830
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0143-9622-01Labetalol Hydrochloride20 mL in 1 VIALINJECTION204
0143-9622-01Labetalol Hydrochloride1 in 1 BOX, UNIT-DOSEINJECTION14

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0143-9622-01ML - Milliliter0143-9622755b3b4b-326e-4e29-9399-9797bfccfc2112017-04-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0143-9622LABETALOL HYDROCHLORIDE INJECTION [HIKMA PHARMACEUTICALS USA INC.]4Current NDC, Legacy NDC, 2 package rows20240711_30f9fdef-8781-4327-9a8d-812cb31ff041.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
896771labetalol HCl 5 MG/ML Injectable SolutionPSN30f9fdef-8781-4327-9a8d-812cb31ff0414
896771labetalol hydrochloride 5 MG/ML Injectable SolutionSCD30f9fdef-8781-4327-9a8d-812cb31ff0414
896771labetalol HCl 5 MG/ML Injectable SolutionPSNe76c4b37-4a34-249d-e053-2995a90aa9be2
896771labetalol hydrochloride 5 MG/ML Injectable SolutionSCDe76c4b37-4a34-249d-e053-2995a90aa9be2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0143-9622-01001439622011 VIAL in 1 BOX, UNIT-DOSE (0143-9622-01) / 20 mL in 1 VIAL1 vial1999-11-290000-00-00NoNoCurrent