23155-847 : Amlodipine and Valsartan Oral Tablet

NDC:	23155-847
Labeler:	Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.
Product Type:	Human Prescription Drug
Drug Name:	Amlodipine and Valsartan
Dosage Form:	Oral Tablet
Application #:	ANDA090011
Rev. Date:	Mar 15, 2023

NDC Package Codes:

23155-847-03: 30 TABLET IN 1 BOTTLE, PLASTIC (23155‑847‑03)
23155-847-09: 90 TABLET IN 1 BOTTLE, PLASTIC (23155‑847‑09)

Active Ingredients:

Amlodipine
Valsartan

Dosage Strength:

10 mg
320 mg

Pharmaceutical Classes:

Angiotensin 2 Receptor Antagonists [MoA]
Angiotensin 2 Receptor Blocker [EPC]
Calcium Channel Antagonists [MoA]
Calcium Channel Blocker [EPC]
Cytochrome P450 3A Inhibitors [MoA]
Dihydropyridine Calcium Channel Blocker [EPC]
Dihydropyridines [CS]

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.