FDA.reportPublic FDA data

Propranolol Hydrochloride

Product NDC
71335-1712
11-digit product format
713351712
Labeler code
71335
Product ID
71335-1712_cf29d6a7-1e9e-478d-ac01-f178a7de9f7b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Propranolol Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA070322
Marketing category
ANDA
Marketing start
2019-10-31
Substance
PROPRANOLOL HYDROCHLORIDE
Active strength
20 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
Propranolol Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PROPRANOLOL HYDROCHLORIDE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF8A3652H1V
Rxcui856457

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ba1babb5-1c2a-d9a8-0fd7-8f90d4f768cfProduct name220200609
a5696e6c-a559-4d6b-bb53-f324106f317cProduct name120140718
0f446d3d-c9e6-1844-b8e8-a836dc35e0deProduct name120140508
33a4b7b4-a3c1-3f95-a202-01166dd77c44Product name120140508
60519d27-227d-404a-38bc-37524c8b386bProduct name120140508
d5f30598-8f94-b083-f161-65d67f2ae12aProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-1712-1Propranolol Hydrochloride20 in 1 BOTTLETABLET20103
71335-1712-2Propranolol Hydrochloride30 in 1 BOTTLETABLET30103
71335-1712-3Propranolol Hydrochloride100 in 1 BOTTLETABLET100103
71335-1712-4Propranolol Hydrochloride60 in 1 BOTTLETABLET60103
71335-1712-5Propranolol Hydrochloride90 in 1 BOTTLETABLET90103
71335-1712-6Propranolol Hydrochloride180 in 1 BOTTLETABLET180103
71335-1712-7Propranolol Hydrochloride28 in 1 BOTTLETABLET28103
71335-1712-8Propranolol Hydrochloride10 in 1 BOTTLETABLET10103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1712PROPRANOLOL HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK]103Current NDC, Legacy NDC, 8 package rows20230404_cf393c74-381f-4b60-8479-b0763bc71e8e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
856457propranolol HCl 20 MG Oral TabletPSNcf393c74-381f-4b60-8479-b0763bc71e8e103
856457propranolol hydrochloride 20 MG Oral TabletSCDcf393c74-381f-4b60-8479-b0763bc71e8e103

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1712-17133517120120 TABLET in 1 BOTTLE (71335-1712-1) 20 tablet2021-12-290000-00-00NoNoCurrent
71335-1712-27133517120230 TABLET in 1 BOTTLE (71335-1712-2) 30 tablet2020-12-300000-00-00NoNoCurrent
71335-1712-371335171203100 TABLET in 1 BOTTLE (71335-1712-3) 100 tablet2021-12-290000-00-00NoNoCurrent
71335-1712-47133517120460 TABLET in 1 BOTTLE (71335-1712-4) 60 tablet2020-11-160000-00-00NoNoCurrent
71335-1712-57133517120590 TABLET in 1 BOTTLE (71335-1712-5) 90 tablet2020-12-010000-00-00NoNoCurrent
71335-1712-671335171206180 TABLET in 1 BOTTLE (71335-1712-6) 180 tablet2021-12-290000-00-00NoNoCurrent
71335-1712-77133517120728 TABLET in 1 BOTTLE (71335-1712-7) 28 tablet2021-12-290000-00-00NoNoCurrent
71335-1712-87133517120810 TABLET in 1 BOTTLE (71335-1712-8) 10 tablet2021-12-290000-00-00NoNoCurrent