amlodipine besylate

Product NDC
59762-1530
11-digit product format
597621530
Labeler code
59762
Product ID
59762-1530_4b488534-377e-4fbb-93fb-3bd140782d3a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
amlodipine besylate
Dosage form
TABLET
Route
ORAL
Labeler
Greenstone LLC
Application
NDA019787
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2007-03-23
Marketing end
2020-03-31
Substance
AMLODIPINE BESYLATE
Active strength
5 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59762-1530-1EA - Each59762-153033f98858-6344-41d0-b915-1de2df042cb512012-07-24
59762-1530-2EA - Each59762-15308a32a6b4-a5fc-43e1-9f0b-8fa4525cb7bb12012-07-24
59762-1530-3EA - Each59762-1530870fd041-5725-4d60-b332-1b412ec7737712012-07-24
59762-1530-4EA - Each59762-153086429126-4c69-4d32-9aff-f6377ab760b912012-07-24
59762-1530-5EA - Each59762-1530b14b19c2-d0b3-4d43-8c7f-14f96486544712012-07-24
59762-1530-6EA - Each59762-1530d3aebcb9-4905-4e50-8e8f-34b2e99e96cd12013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
amlodipine besylateACTIVE INGREDIENT864V2Q084HAMLODIPINE BESYLATE TABLET [REDPHARM DRUG INC.]1
amlodipineACTIVE MOIETY1J444QC288AMLODIPINE BESYLATE TABLET [REDPHARM DRUG INC.]1
anhydrous dibasic calcium phosphateINACTIVE INGREDIENTL11K75P92JAMLODIPINE BESYLATE TABLET [REDPHARM DRUG INC.]1
cellulose, microcrystallineINACTIVE INGREDIENTOP1R32D61UAMLODIPINE BESYLATE TABLET [REDPHARM DRUG INC.]1
magnesium stearateINACTIVE INGREDIENT70097M6I30AMLODIPINE BESYLATE TABLET [REDPHARM DRUG INC.]1
sodium starch glycolate type A potatoINACTIVE INGREDIENT5856J3G2A2AMLODIPINE BESYLATE TABLET [REDPHARM DRUG INC.]1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197361amLODIPine besylate 5 MG Oral TabletPSNd233a645-805b-45be-ae20-534367bc15ff1
197361amlodipine 5 MG Oral TabletSCDd233a645-805b-45be-ae20-534367bc15ff1
197361amlodipine (as amlodipine besylate) 5 MG Oral TabletSYd233a645-805b-45be-ae20-534367bc15ff1