ATORVASTATIN CALCIUM

Product NDC
72162-1555
11-digit product format
721621555
Labeler code
72162
Product ID
72162-1555_4577f7c3-f68a-45fb-927b-c3caabce8f30
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ATORVASTATIN CALCIUM
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA205519
Marketing category
ANDA
Marketing start
2016-05-19
Substance
ATORVASTATIN CALCIUM TRIHYDRATE
Active strength
20 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
ATORVASTATIN CALCIUM
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ATORVASTATIN CALCIUM TRIHYDRATE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii48A5M73Z4Q
Rxcui617310

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fa898d56-9495-d6f0-309b-68a5d8e3914aProduct name420260305
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
d25cba4b-d79e-4890-8837-1382f7d09489Product name120231002
91774e91-b249-45e3-8ff8-4b5db2927a69Product name120230718
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
03fb3cda-d60a-4873-94e9-6fa77cfb1a1cProduct name120220302
34152997-af0b-acf4-dcaf-37211afe8ca4Product name920210312
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
46fdf265-6d5a-1bfb-93db-d82a4ea8aa81Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-1555-5ATORVASTATIN CALCIUM500 in 1 BOTTLETABLET, FILM COATED500102
72162-1555-9ATORVASTATIN CALCIUM90 in 1 BOTTLETABLET, FILM COATED90102

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1555-5EA - Each72162-15554c12c6f5-99f9-4455-bf12-453f127b5b1812024-03-12
72162-1555-9EA - Each72162-155527ade3f9-7c55-46a0-b435-bcf74d0ad24912024-03-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-1555ATORVASTATIN CALCIUM TABLET, FILM COATED [BRYANT RANCH PREPACK]101Current NDC, 2 package rows20240919_5b9a5a36-7814-4d19-b146-01e819676ae2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
617310atorvastatin calcium 20 MG Oral TabletPSN5b9a5a36-7814-4d19-b146-01e819676ae2102
617310atorvastatin 20 MG Oral TabletSCD5b9a5a36-7814-4d19-b146-01e819676ae2102
617310atorvastatin (as atorvastatin calcium) 20 MG Oral TabletSY5b9a5a36-7814-4d19-b146-01e819676ae2102

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
72162-1555-572162155505500 TABLET, FILM COATED in 1 BOTTLE (72162-1555-5) 2016-05-19NoNoHistorical
72162-1555-97216215550990 TABLET, FILM COATED in 1 BOTTLE (72162-1555-9) 2016-05-19NoNoHistorical