Amlodipine Besylate

Product NDC
64679-421
11-digit product format
646790421
Labeler code
64679
Product ID
64679-421_ca52537d-f250-4092-9033-960674a43410
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amlodipine Besylate
Dosage form
TABLET
Route
ORAL
Labeler
Wockhardt USA LLC.
Application
ANDA078500
Marketing category
ANDA
Marketing start
2007-09-06
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
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
64679-421-01EA - Each64679-421965106e5-cd10-4d39-871c-1163f17f2a9412012-07-24
64679-421-02EA - Each64679-4210483864a-781c-416b-9fe4-3d438344be8012022-04-06
64679-421-03EA - Each64679-421679384a2-7c03-4a7a-9dda-c996b8bb46df12022-04-06
64679-421-04EA - Each64679-4214981b763-4c0b-4946-b90c-b3307decd99912022-04-06