Labetalol Hydrochloride

Product NDC
71335-1242
11-digit product format
713351242
Labeler code
71335
Product ID
71335-1242_f2ab8c44-59a2-4c4b-abc1-2e6a4e8b2b5c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Labetalol Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA207743
Marketing category
ANDA
Marketing start
2017-12-05
Substance
LABETALOL HYDROCHLORIDE
Active strength
200 mg/1
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 HYDROCHLORIDE200 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1GEV3BAW9J
Rxcui896762

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
baf61d8c-dcd3-e95d-db84-9bb0d0a2b77fProduct name220220311
759f1c41-9262-4238-8cee-33988631aaf4Product name520220217
3b2edbb4-6acf-4674-b1d9-22addd3dad21Product name120210527

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-1242-1Labetalol Hydrochloride30 in 1 BOTTLETABLET, FILM COATED303
71335-1242-2Labetalol Hydrochloride90 in 1 BOTTLETABLET, FILM COATED903
71335-1242-3Labetalol Hydrochloride60 in 1 BOTTLETABLET, FILM COATED603

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1242LABETALOL HYDROCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK]3Current NDC, Legacy NDC, 3 package rows20230331_9c3bb751-c425-43ff-b530-2460b568b689.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
896762labetalol HCl 200 MG Oral TabletPSN9c3bb751-c425-43ff-b530-2460b568b6893
896762labetalol hydrochloride 200 MG Oral TabletSCD9c3bb751-c425-43ff-b530-2460b568b6893

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-1242-17133512420130 TABLET, FILM COATED in 1 BOTTLE (71335-1242-1) 2019-11-270000-00-00NoNoCurrent
71335-1242-27133512420290 TABLET, FILM COATED in 1 BOTTLE (71335-1242-2) 2021-07-230000-00-00NoNoCurrent
71335-1242-37133512420360 TABLET, FILM COATED in 1 BOTTLE (71335-1242-3) 2019-06-060000-00-00NoNoCurrent