FDA.reportPublic FDA data

Propranolol Hydrochloride

Product NDC
51655-426
11-digit product format
516550426
Labeler code
51655
Product ID
51655-426_48ff25f0-9f7d-30f4-e063-6294a90addbc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Propranolol Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Health Company, LLC
Application
ANDA070322
Marketing category
ANDA
Marketing start
2020-08-27
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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Propranolol Hydrochloride
Listing expiration
2027-12-31

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51655-426-262023-03-27C16284748780-1f386c649-c144-0266-e053-dadaa90a7c1aPROPRANOLOL HYDROCHLORIDE TABLETS, USP Rx
51655-426-522023-03-27C16284748780-1f386c649-c144-0266-e053-dadaa90a7c1aPROPRANOLOL HYDROCHLORIDE TABLETS, USP Rx
51655-426-262023-01-30C16284748780-1f386c649-c144-0266-e053-dadaa90a7c1aPROPRANOLOL HYDROCHLORIDE TABLETS, USP Rx
51655-426-522023-01-30C16284748780-1f386c649-c144-0266-e053-dadaa90a7c1aPROPRANOLOL HYDROCHLORIDE TABLETS, USP Rx

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51655-426-26Propranolol Hydrochloride90 in 1 BOTTLE, PLASTICTABLET903
51655-426-52Propranolol Hydrochloride30 in 1 BOTTLE, PLASTICTABLET303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-426PROPRANOLOL HYDROCHLORIDE TABLET [NORTHWIND PHARMACEUTICALS]2Current NDC, Legacy NDC, 2 package rows20230328_c29d733a-4fcb-6564-e053-2995a90ae541.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
856457propranolol HCl 20 MG Oral TabletPSNc29d733a-4fcb-6564-e053-2995a90ae5413
856457propranolol hydrochloride 20 MG Oral TabletSCDc29d733a-4fcb-6564-e053-2995a90ae5413

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51655-426-265165504262690 TABLET in 1 BOTTLE, PLASTIC (51655-426-26) 90 tablet2021-01-140000-00-00NoNoCurrent
51655-426-525165504265230 TABLET in 1 BOTTLE, PLASTIC (51655-426-52) 30 tablet2020-08-270000-00-00NoNoCurrent