FDA.reportPublic FDA data

Amlodipine Besylate

Product NDC
69097-836
11-digit product format
690970836
Labeler code
69097
Product ID
69097-836_adb955ec-2369-441f-9db6-0a22bb5b2e7e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amlodipine Besylate
Dosage form
TABLET
Route
ORAL
Labeler
Cipla USA Inc.
Application
ANDA077955
Marketing category
ANDA
Marketing start
2016-07-01
Substance
AMLODIPINE BESYLATE
Active strength
2.5 mg/1
Pharmacologic classes
Calcium Channel Antagonists [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 BESYLATE2.5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii864V2Q084H
Rxcui197361, 308135, 308136

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
69097-836-05Amlodipine Besylate90 in 1 BOTTLETABLET906
69097-836-15Amlodipine Besylate1000 in 1 BOTTLETABLET10006

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69097-836-05EA - Each69097-836cc6d73ba-9728-4922-979b-06e7df4cfead12016-07-19
69097-836-15EA - Each69097-83698314091-c439-415d-9c92-0ffdcb5d4bcd12016-07-19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69097-836AMLODIPINE BESYLATE TABLET [CIPLA USA INC.]6Current NDC, Legacy NDC, 2 package rows20201022_0c8d6b2f-3e4a-47a2-80e2-a34dcb337555.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308135amLODIPine besylate 10 MG Oral TabletPSN0c8d6b2f-3e4a-47a2-80e2-a34dcb3375556
308136amLODIPine besylate 2.5 MG Oral TabletPSN0c8d6b2f-3e4a-47a2-80e2-a34dcb3375556
197361amLODIPine besylate 5 MG Oral TabletPSN0c8d6b2f-3e4a-47a2-80e2-a34dcb3375556
308135amlodipine 10 MG Oral TabletSCD0c8d6b2f-3e4a-47a2-80e2-a34dcb3375556
308136amlodipine 2.5 MG Oral TabletSCD0c8d6b2f-3e4a-47a2-80e2-a34dcb3375556
197361amlodipine 5 MG Oral TabletSCD0c8d6b2f-3e4a-47a2-80e2-a34dcb3375556
308135amlodipine (as amlodipine besylate) 10 MG Oral TabletSY0c8d6b2f-3e4a-47a2-80e2-a34dcb3375556
308136amlodipine (as amlodipine besylate) 2.5 MG Oral TabletSY0c8d6b2f-3e4a-47a2-80e2-a34dcb3375556
197361amlodipine (as amlodipine besylate) 5 MG Oral TabletSY0c8d6b2f-3e4a-47a2-80e2-a34dcb3375556

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69097-836-056909708360590 TABLET in 1 BOTTLE (69097-836-05) 90 tablet2016-07-010000-00-00NoNoCurrent
69097-836-15690970836151000 TABLET in 1 BOTTLE (69097-836-15) 1000 tablet2016-07-010000-00-00NoNoCurrent