Home NDC 16729-393 NDC 16729-393 - amlodipine besylate and olmesartan medoxomil This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 16729-393
Package NDCs from labels 16729-393-10, 16729-393-15, 16729-393-16, 16729-393-17
Manufacturer Accord Healthcare Inc. | Intas Pharmaceuticals Limited
Effective date 2019-08-14
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 16729-393-10 amlodipine besylate and olmesartan medoxomil 30 in 1 BOTTLE TABLET, FILM COATED 30 2 16729-393-15 amlodipine besylate and olmesartan medoxomil 90 in 1 BOTTLE TABLET, FILM COATED 90 2 16729-393-16 amlodipine besylate and olmesartan medoxomil 500 in 1 BOTTLE TABLET, FILM COATED 500 2 16729-393-17 amlodipine besylate and olmesartan medoxomil 1000 in 1 BOTTLE TABLET, FILM COATED 1000 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 16729-393 AMLODIPINE BESYLATE AND OLMESARTAN MEDOXOMIL TABLET, FILM COATED [ACCORD HEALTHCARE INC.] 2 4 package rows 20220901_a855ce60-6918-490a-9158-3be5a0ef76b5.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 113 of 123 · 2,441 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.