FDA.reportPublic FDA data

NDC 58407-025-01 - AHIST

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
58407-025
Requested NDC
58407-025-01
Package NDCs from labels
58407-025-01, 58407-025-30, 58407-025-06
Manufacturer
Magna Pharmaceutcals, Inc.
Effective date
2022-08-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
AHIST™Magna Pharmaceutcals, Inc.2022-08-17HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
58407-025-062023-07-28AHIST™
58407-025-302023-07-28AHIST™
58407-025-062022-08-17AHIST™
58407-025-302022-08-17AHIST™
58407-025-062021-01-29AHIST™
58407-025-302021-01-29AHIST™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58407-025-01AHIST1 in 1 BLISTER PACKTABLET14
58407-025-06AHIST6 in 1 BOXTABLET64
58407-025-30AHIST30 in 1 BOXTABLET304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58407-025AHIST (CHLORCYCLIZINE HYDROCHLORIDE) TABLET [MAGNA PHARMACEUTCALS, INC.]4Legacy NDC, 3 package rows20220819_d50b5154-20a3-4c5b-ad7b-08c081340b12.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
58407-025-01EA - Each58407-025eed65d21-07a4-4b36-9602-d7195ff4a61912022-06-06
58407-025-30EA - Each58407-0258b9cd244-5c50-4208-a7ef-bd7b0cc53cbf12013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHLORCYCLIZINE HYDROCHLORIDEACTIVE INGREDIENTNPB7A7874UAHIST (CHLORCYCLIZINE HYDROCHLORIDE) TABLET [MAGNA PHARMACEUTCALS, INC.]1
CHLORCYCLIZINEACTIVE MOIETYM26C4IP44PAHIST (CHLORCYCLIZINE HYDROCHLORIDE) TABLET [MAGNA PHARMACEUTCALS, INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UAHIST (CHLORCYCLIZINE HYDROCHLORIDE) TABLET [MAGNA PHARMACEUTCALS, INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30AHIST (CHLORCYCLIZINE HYDROCHLORIDE) TABLET [MAGNA PHARMACEUTCALS, INC.]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2AHIST (CHLORCYCLIZINE HYDROCHLORIDE) TABLET [MAGNA PHARMACEUTCALS, INC.]1

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 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
STAHIST ADCHLORCYCLIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDEMagna Pharmaceuticals, Inc.ccedbc38-2479-4c35-9f86-a9f29bcfab3f2025-10-03WarningsExact identifier
unii: NPB7A7874U
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U
938dae00-2ce6-40bc-84a5-45407d327bc1d50b5154-20a3-4c5b-ad7b-08c081340b122022-08-17WarningsExact identifier
spl id: 938dae00-2ce6-40bc-84a5-45407d327bc1
spl set id: d50b5154-20a3-4c5b-ad7b-08c081340b12

Reported adverse events (FAERS/openFDA)#

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