FDA.reportPublic FDA data

Amlodipine besylate

Product NDC
63629-1024
11-digit product format
636291024
Labeler code
63629
Product ID
63629-1024_ff242576-5fe6-4693-933a-ae9721e7c3a3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amlodipine besylate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077955
Marketing category
ANDA
Marketing start
2007-11-02
Substance
AMLODIPINE BESYLATE
Active strength
5 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Amlodipine besylate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMLODIPINE BESYLATE5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii864V2Q084H
Rxcui197361

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fa898d56-9495-d6f0-309b-68a5d8e3914aProduct name420260305
c19ec24d-2c40-4b8d-7c20-500ffa3660a1Product name320260303
b15e9aa6-d523-ca97-480e-570e0543a342Product name420251024
265792b3-b999-c010-7364-a7db20b9d4d9Product name520250515
14c2c15b-f823-4ada-a40e-a440544294dcProduct name120221207
a72887ef-d675-499f-af4b-78688f6855cdProduct name120191002
a4484670-2869-6416-f6ff-03b1b3cbd1b0Product name220190415
4a27501f-a987-48a5-99b4-e983d4744d76Product name720181211
18600d07-613d-bf9c-2711-fe40c06f3393Product name520180703
bded1554-44de-900a-5297-403365d6d4b2Product name320170110
1f1c6e4b-bbad-4649-afd1-7a1d671db4b1Product name120150316
63ab5fbf-2a6b-c41d-051a-39e845d718b1Product name120140508
7613b1a5-acb6-4e5e-6048-c44deeeb1212Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63629-1024-2Amlodipine besylate30 in 1 BOTTLETABLET307
63629-1024-3Amlodipine besylate300 in 1 BOTTLETABLET3007
63629-1024-5Amlodipine besylate500 in 1 BOTTLETABLET5007
63629-1024-6Amlodipine besylate60 in 1 BOTTLETABLET607
63629-1024-8Amlodipine besylate800 in 1 BOTTLETABLET8007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63629-1024AMLODIPINE BESYLATE TABLET [BRYANT RANCH PREPACK]7Current NDC, Legacy NDC, 5 package rows20240110_e8958997-f098-44ce-8c21-b7064d1a962e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197361amLODIPine besylate 5 MG Oral TabletPSNe8958997-f098-44ce-8c21-b7064d1a962e7
197361amlodipine 5 MG Oral TabletSCDe8958997-f098-44ce-8c21-b7064d1a962e7
197361amlodipine (as amlodipine besylate) 5 MG Oral TabletSYe8958997-f098-44ce-8c21-b7064d1a962e7

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-1024-26362910240230 TABLET in 1 BOTTLE (63629-1024-2) 30 tablet2022-01-030000-00-00NoNoCurrent
63629-1024-363629102403300 TABLET in 1 BOTTLE (63629-1024-3) 300 tablet2022-01-030000-00-00NoNoCurrent
63629-1024-563629102405500 TABLET in 1 BOTTLE (63629-1024-5) 500 tablet2022-01-030000-00-00NoNoCurrent
63629-1024-66362910240660 TABLET in 1 BOTTLE (63629-1024-6) 60 tablet2022-01-030000-00-00NoNoCurrent
63629-1024-863629102408800 TABLET in 1 BOTTLE (63629-1024-8) 800 tablet2022-01-030000-00-00NoNoCurrent