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 8 of 36 · 705 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BIO COM 25 ACIDITYNAT PHOS, NAT SULPH, SILICEABM Private Limited3b3c3455-b321-071d-e063-6394a90a01602026-02-17WarningsExact identifier
unii: ETJ7Z6XBU4
GlipizideGLIPIZIDEPD-Rx Pharmaceuticals, Inc.f60b0690-aca9-40ec-956e-bd2ecc35ec542026-02-16Warnings, Adverse reactionsExact identifier
application number: ANDA075795
rxcui: 310490
unii: X7WDT95N5C
CINAAMBROSIA, CINA, CUCURBITA CIT, CUCURBITA PEP, INDIGO, SANTONINE, SILICEABM PRIVATE LIMITED3b3c0874-90b5-deda-e063-6394a90a78022026-02-15WarningsExact identifier
unii: ETJ7Z6XBU4
Acne/Pimple ControlCALENDULA OFFICINALIS FLOWERING TOP AND SILICON DIOXIDEForces of Naturee871e46e-463e-49ec-a2af-5aa98548ee122026-02-13WarningsExact identifier
unii: ETJ7Z6XBU4
FuligoCIMICIFUGA, DROSERA, FORMICA RUFA, FULIGO, INULA HEL., KALI MUR, LAPIS ALBUS, SILICEABM Private Limited3b27225f-4587-d915-e063-6294a90a72252026-02-12WarningsExact identifier
unii: ETJ7Z6XBU4
GlipizideGLIPIZIDEA-S Medication Solutions383540fd-2931-49bf-8009-25e8f7fc9bda2026-02-10Warnings, Adverse reactionsExact identifier
application number: ANDA075795
unii: X7WDT95N5C
GlipizideGLIPIZIDEA-S Medication Solutionsa38cfe61-4aa5-498c-bca5-03a8213303bb2026-02-10Warnings, Adverse reactionsExact identifier
application number: ANDA075795
unii: X7WDT95N5C
Mold, Yeast and DustADRENALINUM, ARSENICUM IODATUM, ASPERGILLUS FLAVUS, ASPERGILLUS FUMIGATUS, ASPERGILLUS GLAUCUS, ASPERGILLUS NIDULANS, ASPERGILLUS NIGER, CANDIDA ALBICANS, DERMATOPHAGOIDES FARINAE, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, MUCOR PLUMBEUS, NATRUM SULPHURICUM, PENICILLIUM DIGITATUM, PENICILLIUM ROQUEFORTII, SACCHAROMYCES CEREVISIAE, SILICEANaturalCare32afa0f0-bca5-4246-bc2e-decd757fcf9d2026-02-09WarningsExact identifier
unii: ETJ7Z6XBU4
DPT-TOXDROSERA, ECHINACEA, HYPERICUM, KALI MUR, MEZEREUM, SILICEA, THUJANutrition Center Inc dba Nutri-West dba Micro-West5e39f4e6-939f-4b71-9cc5-6d4b8711ea322026-02-04WarningsExact identifier
unii: ETJ7Z6XBU4
GlipizideGLIPIZIDEREMEDYREPACK INC.bde478e6-e290-47e0-9241-ce88d927633e2026-02-04Warnings, Adverse reactionsExact identifier
unii: X7WDT95N5C
Meteoric Iron PrunusMETEORIC IRON PRUNUSUriel Pharmacy Inc.e9020757-2393-4a22-9665-25da0a0993d02026-02-03WarningsExact identifier
unii: ETJ7Z6XBU4
Mold, Yeast and DustACREMONIUM STRICTUM, ADRENALINUM, ALLIUM CEPA, ALTERNARIA ALTERNATA, ARSENICUM IODATUM, ASPERGILLUS FUMIGATUS, ASPERGILLUS NIGER, AUREOBASIDIUM PULLULANS, CANDIDA ALBICANS, CLADOSPORIUM HERBARUM, COCKROACH, DERMATOPHAGOIDES FARINAE, EPICOCCUM PURPURASCENS, FUSARIUM SOLANI, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, MUCOR CIRCINELLOIDES, NATRUM SULPHURICUM, RHIZOPUS STOLONIFER, SACCHAROMYCES CEREVISIAE, SILICEANaturalCaree0f53f47-acd9-43e2-a7a2-2a500bc9dc1b2026-02-03WarningsExact identifier
unii: ETJ7Z6XBU4
GlipizideGLIPIZIDEPreferred Pharmaceuticals Inc.410bf280-838d-45af-9b60-15f94ded75812026-01-28Warnings, Adverse reactionsExact identifier
unii: X7WDT95N5C
BioMicroneedle PDRN CreamSILICON DIOXIDEGuangzhou Shengyanghui Industrial Trading Co., Ltd48e2edae-94ea-c42e-e063-6394a90a907b2026-01-21WarningsExact identifier
unii: ETJ7Z6XBU4
Inflammation IECHINACEA (ANGUSTIFOLIA), NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, APIS MELLIFICA, BELLADONNA, FERRUM PHOSPHORICUM, NITRICUM ACIDUM, OLEANDER, SILICEABioActive Nutritional, Inc.3cb12181-ae7e-45c7-a1b1-e1952f36f8c32026-01-21WarningsExact identifier
unii: ETJ7Z6XBU4
GlipizideGLIPIZIDENorthwind Health Company, LLC0ed5ed22-dd53-495d-bc10-0bede4d879262026-01-19Warnings, Adverse reactionsExact identifier
application number: ANDA075795
unii: X7WDT95N5C
GlipizideGLIPIZIDERising Pharma Holdings, Inc.0ffe361a-c99b-4f68-a7e2-a67a71c0c4962026-01-17Warnings, Adverse reactionsExact identifier
unii: X7WDT95N5C
DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTHSILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATEATOSAFE CO., Ltd487c5036-0eb0-ada9-e063-6394a90aa02e2026-01-16WarningsExact identifier
unii: ETJ7Z6XBU4
DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTHSILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATEDONG IL PHARMS CO.,LTD487cd5b9-28f3-392d-e063-6394a90a9ba12026-01-16WarningsExact identifier
unii: ETJ7Z6XBU4
DENTI BUONGIORNO GUM CARE COOL MINT TOOTHSILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATEATOSAFE CO., Ltd487cf27a-d761-6353-e063-6394a90af0292026-01-16WarningsExact identifier
unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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