FDA.reportPublic FDA data

AMLODIPINE BESYLATE

Product NDC
61919-753
11-digit product format
619190753
Labeler code
61919
Product ID
61919-753_b933a6b2-634c-39a9-e053-2a95a90a8417
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
AMLODIPINE BESYLATE
Dosage form
TABLET
Route
ORAL
Labeler
DIRECT RX
Application
ANDA077073
Marketing category
ANDA
Marketing start
2021-01-18
Marketing end
0000-00-00
Substance
AMLODIPINE BESYLATE
Active strength
3 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61919-753-902025-01-30C16284748780-19d75b9cf-fd64-f424-e053-dadaa90a57ceAMLODIPINE BESYLATE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61919-753-90AMLODIPINE BESYLATE90 in 1 BOTTLETABLET903

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
61919-753-90EA - Each61919-753b327c9cc-3955-45db-b7d1-42e59ac3dd9d12021-02-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61919-753AMLODIPINE BESYLATE TABLET [DIRECT RX]3Legacy NDC, 1 package rows20210119_48f94245-3a9d-0b7c-e054-00144ff88e88.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308135amLODIPine besylate 10 MG Oral TabletPSN48f94245-3a9d-0b7c-e054-00144ff88e883
308136amLODIPine besylate 2.5 MG Oral TabletPSN48f94245-3a9d-0b7c-e054-00144ff88e883
308135amlodipine 10 MG Oral TabletSCD48f94245-3a9d-0b7c-e054-00144ff88e883
308136amlodipine 2.5 MG Oral TabletSCD48f94245-3a9d-0b7c-e054-00144ff88e883
308135amlodipine (as amlodipine besylate) 10 MG Oral TabletSY48f94245-3a9d-0b7c-e054-00144ff88e883
308136amlodipine (as amlodipine besylate) 2.5 MG Oral TabletSY48f94245-3a9d-0b7c-e054-00144ff88e883

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61919-753-906191907539090 TABLET in 1 BOTTLE (61919-753-90) 90 tablet2021-01-180000-00-00NoNoCurrent