Home NDC 70710-1133-01 NDC 70710-1133-01 - Chlorpromazine hydrochloride 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 70710-1133
Requested NDC 70710-1133-01
Package NDCs from labels 70710-1133-1, 70710-1133-2, 70710-1133-4, 70710-1133-01
Manufacturer Major Pharmaceuticals
Effective date 2025-11-11
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 70710-1133-1 Chlorpromazine hydrochloride 100 in 1 BOTTLE TABLET, FILM COATED 100 5 70710-1133-2 Chlorpromazine hydrochloride 10 in 1 BLISTER PACK TABLET, FILM COATED 10 5 70710-1133-4 Chlorpromazine hydrochloride 10 in 1 CARTON TABLET, FILM COATED 10 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70710-1133 CHLORPROMAZINE HYDROCHLORIDE TABLET, FILM COATED [ZYDUS PHARMACEUTICALS (USA) INC.] 5 Current NDC, Legacy NDC, 3 package rows 20240814_fc2bd95d-a7bc-4ab5-bffa-f5059cb8eb63.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 125 of 137 · 2,722 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.