Amlodipine Besylate

Product NDC: 50090-1021
11-digit product format: 500901021
Labeler code: 50090
Product ID: 50090-1021_c1df8199-52c0-44a9-b166-3d6317a646f5
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: amlodipine besylate
Dosage form: TABLET
Route: ORAL
Labeler: A-S Medication Solutions
Application: ANDA078414
Marketing category: ANDA
Marketing start: 2010-04-07
Marketing end: 0000-00-00
Substance: AMLODIPINE BESYLATE
Active strength: 10 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#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50090-1021-0	2020-01-31	C162847	48780-1	9d75b9d0-c68e-f424-e053-dadaa90a57ce	6c8a6b0f-d19f-470d-aacf-bd3ee638f7db
50090-1021-1	2020-01-31	C162847	48780-1	9d75b9d0-c68e-f424-e053-dadaa90a57ce	6c8a6b0f-d19f-470d-aacf-bd3ee638f7db

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50090-1021	AMLODIPINE BESYLATE TABLET [A-S MEDICATION SOLUTIONS]	4	Legacy NDC	20171108_6c8a6b0f-d19f-470d-aacf-bd3ee638f7db.zip