NDC 0143-9433-01 - Acetylcysteine

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
0143-9433
Requested NDC
0143-9433-01
Package NDCs from labels
0143-9433-01, 0143-9433-04
Manufacturer
Hikma Pharmaceuticals USA Inc. | ONESOURCE SPECIALTY PHARMA LIMITED
Effective date
2025-09-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Acetylcysteine - Hikma Pharmaceuticals USA Inc. | ONESOURCE SPECIALTY PHARMA LIMITEDHikma Pharmaceuticals USA Inc. | ONESOURCE SPECIALTY PHARMA LIMITED2025-09-09HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0143-9433-01Acetylcysteine30 mL in 1 VIALINJECTION, SOLUTION301
0143-9433-04Acetylcysteine4 in 1 CARTONINJECTION, SOLUTION41

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0143-9433-01ML - Milliliter0143-94334025225a-b7ed-4873-a0cd-91301bcaee7c12026-04-20
0143-9433-04ML - Milliliter0143-9433e58fe1da-c605-4e0f-954a-62dbcf75ae0612026-04-20

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 2 of 2 · 22 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcetylcysteineACETYLCYSTEINESagent Pharmaceuticals2324d60b-4f49-4759-a46e-a06bfce7e8aa2022-04-05Warnings, Adverse reactionsExact identifier
rxcui: 465377
unii: WYQ7N0BPYC
ACETYLCYSTEINEACETYLCYSTEINEIndoco Remedies Limited6588c28d-0515-4cdf-99d3-c4ad3fd0976c2022-03-01Warnings, Adverse reactionsExact identifier
rxcui: 465377
unii: WYQ7N0BPYC

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.