FDA.reportPublic FDA data

Amlodipine Besylate

Product NDC
50090-6808
11-digit product format
500906808
Labeler code
50090
Product ID
50090-6808_01a4a136-ecab-4c98-a853-c5750e70605b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amlodipine Besylate
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA203245
Marketing category
ANDA
Marketing start
2019-05-22
Substance
AMLODIPINE BESYLATE
Active strength
10 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 BESYLATE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii864V2Q084H
Rxcui308135

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
50090-6808-0Amlodipine Besylate30 in 1 BOTTLETABLET301
50090-6808-1Amlodipine Besylate90 in 1 BOTTLETABLET901
50090-6808-2Amlodipine Besylate100 in 1 BOTTLETABLET1001

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-6808-0EA - Each50090-6808f4e7d190-254f-42b8-af4c-d53ed68462e212023-12-05
50090-6808-1EA - Each50090-6808da4b7a20-9248-4cfd-be15-143ecce522d312023-12-05
50090-6808-2EA - Each50090-6808ec52dcb7-a6dd-4e17-8e32-cdfbf760e6ad12023-12-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-6808AMLODIPINE BESYLATE TABLET [A-S MEDICATION SOLUTIONS]1Current NDC, 3 package rows20231115_5c50c3fe-afe5-459e-95c0-c9af4cbb6909.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308135amLODIPine besylate 10 MG Oral TabletPSN5c50c3fe-afe5-459e-95c0-c9af4cbb69091
308135amlodipine 10 MG Oral TabletSCD5c50c3fe-afe5-459e-95c0-c9af4cbb69091
308135amlodipine (as amlodipine besylate) 10 MG Oral TabletSY5c50c3fe-afe5-459e-95c0-c9af4cbb69091

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
50090-6808-05009068080030 TABLET in 1 BOTTLE (50090-6808-0) 30 tablet2023-11-07NoNoCurrent
50090-6808-15009068080190 TABLET in 1 BOTTLE (50090-6808-1) 90 tablet2023-11-07NoNoCurrent
50090-6808-250090680802100 TABLET in 1 BOTTLE (50090-6808-2) 100 tablet2023-11-07NoNoCurrent