FDA.reportPublic FDA data

AMLODIPINE BESYLATE

Product NDC
70518-0835
11-digit product format
705180835
Labeler code
70518
Product ID
70518-0835_4d664c6a-08f3-91bd-e063-6394a90aac1c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
AMLODIPINE BESYLATE
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA077073
Marketing category
ANDA
Marketing start
2017-11-10
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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
AMLODIPINE BESYLATE
Listing expiration
2027-12-31

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
70518-0835-0AMLODIPINE BESYLATE30 in 1 BOTTLE, PLASTICTABLET3015
70518-0835-1AMLODIPINE BESYLATE90 in 1 BOTTLE, PLASTICTABLET9015
70518-0835-2AMLODIPINE BESYLATE100 in 1 BOTTLE, PLASTICTABLET10015
70518-0835-3AMLODIPINE BESYLATE30 in 1 BLISTER PACKTABLET3015

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197361amLODIPine besylate 5 MG Oral TabletPSNd09173a1-5e3c-4c86-8c7c-15238925ef5015
197361amlodipine 5 MG Oral TabletSCDd09173a1-5e3c-4c86-8c7c-15238925ef5015
197361amlodipine (as amlodipine besylate) 5 MG Oral TabletSYd09173a1-5e3c-4c86-8c7c-15238925ef5015

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-0835-07051808350030 TABLET in 1 BOTTLE, PLASTIC (70518-0835-0) 30 tablet2017-11-100000-00-00NoNoCurrent
70518-0835-17051808350190 TABLET in 1 BOTTLE, PLASTIC (70518-0835-1) 90 tablet2018-06-180000-00-00NoNoCurrent
70518-0835-270518083502100 TABLET in 1 BOTTLE, PLASTIC (70518-0835-2) 100 tablet2020-10-300000-00-00NoNoCurrent
70518-0835-37051808350330 TABLET in 1 BLISTER PACK (70518-0835-3) 30 tablet2023-06-08NoNoCurrent