FDA.reportPublic FDA data

NDC 50090-0502-01 - Glipizide

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
50090-0502
Requested NDC
50090-0502-01
Package NDCs from labels
50090-0502-0, 50090-0502-3, 50090-0502-4, 50090-0502-1, 50090-0502-2, 50090-0502-01
Manufacturer
A-S Medication Solutions
Effective date
2026-10-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Glipizide - A-S Medication SolutionsA-S Medication Solutions2026-10-13HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
50090-0502-02023-02-07GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-02023-02-07GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-12023-02-07GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-12023-02-07GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-22023-02-07GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-22023-02-07GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-32023-02-07GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-32023-02-07GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-42023-02-07GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-42023-02-07GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-02023-01-30GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-02023-01-30GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-12023-01-30GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-12023-01-30GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-22023-01-30GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-22023-01-30GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-32023-01-30GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-32023-01-30GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-42023-01-30GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only
50090-0502-42023-01-30GLIPIZIDE TABLETS, USP 5 mg and 10 mg Rx Only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-0502-0Glipizide30 in 1 BOTTLETABLET3015
50090-0502-1Glipizide60 in 1 BOTTLETABLET6015
50090-0502-2Glipizide100 in 1 BOTTLETABLET10015
50090-0502-3Glipizide90 in 1 BOTTLETABLET9015
50090-0502-4Glipizide180 in 1 BOTTLETABLET18015

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-0502GLIPIZIDE TABLET [A-S MEDICATION SOLUTIONS]13Current NDC, Legacy NDC, 5 package rows20231110_16fb8bc7-1db1-477e-a201-b3b678b8a84c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-0502-0EA - Each50090-0502b68ff126-b7e7-4b66-80da-4727383ad05912018-09-05
50090-0502-1EA - Each50090-0502faa317f1-ddb3-4440-a2eb-355284e6886f12018-09-05
50090-0502-2EA - Each50090-0502d14746df-555d-40be-9d6e-0600429b179d12018-09-05
50090-0502-3EA - Each50090-050286eaeaab-6d5d-431f-a72a-0130b6f4bb2c12018-09-05
50090-0502-4EA - Each50090-0502b4fc27fd-e13d-4cf5-9790-3d2505b0c75a12018-09-05

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 35 of 35 · 683 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Tox-ChordALFALFA, ALUMINA, BENZOICUM ACIDUM, CARBONEUM, CETRARIA ISLANDICA, FOLLICULINUM, FUCUS VESICULOSUS, FUMARICUM ACIDUM, HEPAR SUIS, KALI CARBONICUM, KREOSOTUM, NATRUM MURIATICUM, PARAFFINUM, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PIX LIQUIDA, PLANTAGO MAJOR, PLUMBUM METALLICUM, PULSATILLA (VULGARIS), RADIUM BROMATUM, RESORCINUM, SALOL, SILICEA, SYMPHYTUM OFFICINALE, TABACUM, TEREBINTHINA, THYROIDINUM (BOVINE), TRITICUM REPENS, ZINCUM OXYDATUMEnergetix Corp6b0d1628-b20d-426e-9c84-5cceadca3f452016-11-11WarningsExact identifier
unii: ETJ7Z6XBU4
ThyrotoxCHONDRUS CRISPUS, FUCUS VESICULOSUS, THYROIDINUM, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, IODIUM, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (VULGARIS), SILICEABioActive Nutritional, Inc.e229a260-13f3-4136-b325-9a8954f8a3272016-08-10WarningsExact identifier
unii: ETJ7Z6XBU4
TeethingARNICA MONTANA, TRIFOLIUM PRATENSE, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CHAMOMILLA, KREOSOTUM, SILICEABioActive Nutritional, Inc.f39c9feb-f567-43a2-a026-2a581aeeed9d2016-07-27WarningsExact identifier
unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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