Pindolol

Product NDC
57664-655
11-digit product format
576640655
Labeler code
57664
Product ID
57664-655_4d3c89dd-e947-5f23-e063-6294a90aeb1f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pindolol
Dosage form
TABLET
Route
ORAL
Labeler
Sun Pharmaceutical Industries, Inc.
Application
ANDA074063
Marketing category
ANDA
Marketing start
1994-01-27
Marketing end
2027-01-31
Substance
PINDOLOL
Active strength
5 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Pindolol

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PINDOLOL5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiBJ4HF6IU1D
Rxcui198104, 198105

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
741bb9aa-d388-e012-0ad7-8a85bcbe396eProduct name420200121

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57664-655-88Pindolol100 in 1 BOTTLE, PLASTICTABLET1007

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
57664-655-88EA - Each57664-655636de6ba-cb9b-4db1-8c24-e42d45251c1612014-05-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PindololACTIVE INGREDIENTBJ4HF6IU1DPINDOLOL TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.]2
PindololACTIVE MOIETYBJ4HF6IU1DPINDOLOL TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.]2
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMKPINDOLOL TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UPINDOLOL TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.]2
CROSPOVIDONEINACTIVE INGREDIENT68401960MKPINDOLOL TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30PINDOLOL TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJPINDOLOL TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57664-655PINDOLOL TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.]6Current NDC, Legacy NDC, 1 package rows20210213_b331a73f-bf7b-4442-8901-36d016530279.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198105pindolol 5 MG Oral TabletPSN79a8d97b-9461-4914-bcbb-f6f64a39e5e79
198105pindolol 5 MG Oral TabletSCD79a8d97b-9461-4914-bcbb-f6f64a39e5e79
198104pindolol 10 MG Oral TabletPSNb331a73f-bf7b-4442-8901-36d0165302797
198105pindolol 5 MG Oral TabletPSNb331a73f-bf7b-4442-8901-36d0165302797
198104pindolol 10 MG Oral TabletSCDb331a73f-bf7b-4442-8901-36d0165302797
198105pindolol 5 MG Oral TabletSCDb331a73f-bf7b-4442-8901-36d0165302797

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
57664-655-8857664065588100 TABLET in 1 BOTTLE, PLASTIC (57664-655-88) 100 tablet1994-01-272027-01-31NoNoCurrent