FDA.reportPublic FDA data

Glimepiride

Product NDC
42571-103
11-digit product format
425710103
Labeler code
42571
Product ID
42571-103_34e9a6b6-450b-7d20-e063-6294a90ac831
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glimepiride
Dosage form
TABLET
Route
ORAL
Labeler
Micro Labs Limited
Application
ANDA091220
Marketing category
ANDA
Marketing start
2013-06-13
Substance
GLIMEPIRIDE
Active strength
4 mg/1
Pharmacologic classes
Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 6 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A091220-001GLIMEPIRIDEGLIMEPIRIDE1MGTABLET / ORALAB2012-06-29
A091220-002GLIMEPIRIDEGLIMEPIRIDE2MGTABLET / ORALAB2012-06-29
A091220-003GLIMEPIRIDEGLIMEPIRIDE3MGTABLET / ORAL2012-06-29
A091220-004GLIMEPIRIDEGLIMEPIRIDE4MGTABLET / ORALAB2012-06-29
A091220-005GLIMEPIRIDEGLIMEPIRIDE6MGTABLET / ORAL2012-06-29
A091220-006GLIMEPIRIDEGLIMEPIRIDE8MGTABLET / ORALAB2012-06-29

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 4 matching rows.

Application-product, TE code table
Application-productTE code
A091220-001AB
A091220-002AB
A091220-004AB
A091220-006AB

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-08-01 22:54:322026-06A091220-001GLIMEPIRIDE1MGTABLET / ORALAB2012-06-29a50c72e98297…
2026-08-01 22:54:322026-06A091220-002GLIMEPIRIDE2MGTABLET / ORALAB2012-06-29a50c72e98297…
2026-08-01 22:54:322026-06A091220-003GLIMEPIRIDE3MGTABLET / ORAL2012-06-29a50c72e98297…
2026-08-01 22:54:322026-06A091220-004GLIMEPIRIDE4MGTABLET / ORALAB2012-06-29a50c72e98297…
2026-08-01 22:54:322026-06A091220-005GLIMEPIRIDE6MGTABLET / ORAL2012-06-29a50c72e98297…
2026-08-01 22:54:322026-06A091220-006GLIMEPIRIDE8MGTABLET / ORALAB2012-06-29a50c72e98297…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-08-01 22:54:322026-06A091220-001AB1a50c72e98297…
2026-08-01 22:54:322026-06A091220-002AB1a50c72e98297…
2026-08-01 22:54:322026-06A091220-004AB1a50c72e98297…
2026-08-01 22:54:322026-06A091220-006AB1a50c72e98297…

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 6 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GlimepirideGLIMEPIRIDEBryant Ranch Prepack62780d2e-083d-4bcb-99ff-1b1b4ade60d92026-03-09Warnings, Adverse reactionsExact identifier
application applno (ANDA): 091220
application number: ANDA091220
GlimepirideGLIMEPIRIDEBluePoint Laboratoriesa01b0466-13f5-4c47-ae55-c5f1527d94142025-07-07Warnings, Adverse reactionsExact identifier
application applno (ANDA): 091220
application number: ANDA091220
GlimepirideGLIMEPIRIDEBryant Ranch Prepackd4513181-4558-4d9a-851b-acf7e3eda25a2025-06-16Warnings, Adverse reactionsExact identifier
application applno (ANDA): 091220
application number: ANDA091220
GlimepirideGLIMEPIRIDEMicro Labs Limited60e9397e-83b9-489e-9683-6f87e458bbaa2025-05-12Warnings, Adverse reactionsExact identifier
application applno (ANDA): 091220
application number: ANDA091220
ndc (product): 42571-103
Glimepiride 3 mgGLIMEPIRIDELifsa Drugs LLC51157849-7990-4a8b-ae50-eda1baf93cfa2024-08-20Warnings, Adverse reactionsExact identifier
application applno (ANDA): 091220
application number: ANDA091220
GlimepirideGLIMEPIRIDENCS HealthCare of KY, Inc dba Vangard Labs669a67c2-2f97-4b7e-8bba-83a015e0fa942020-04-30Warnings, Adverse reactionsExact identifier
application applno (ANDA): 091220
application number: ANDA091220

Additional Listing Data#

Finished product
Yes
Brand name base
Glimepiride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GLIMEPIRIDE4 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
6KY687524KInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 6 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
153842Internal RxNorm lookup
199245Internal RxNorm lookup
199246Internal RxNorm lookup
199247Internal RxNorm lookup
1361493Internal RxNorm lookup
1361495Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
60e9397e-83b9-489e-9683-6f87e458bbaaAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b890b964-2cf0-4439-aaf3-900c9e3e9e49Product name120160602
7611093e-8875-33d4-9e3c-f48c7e3af1e8Product name120140508
d36d861f-8a90-80cc-8935-1e6be9b4c7ebProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42571-103-01Glimepiride100 in 1 BOTTLETABLET10091233
42571-103-05Glimepiride500 in 1 BOTTLETABLET50091233

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42571-103-01EA - Each42571-1038d14c87b-8508-4578-a921-61ebce73dfa612013-04-01
42571-103-05EA - Each42571-103f58a41a7-6d06-42c3-b405-13cdfeff56f912013-12-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GLIMEPIRIDEACTIVE INGREDIENT6KY687524KGLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224
GLIMEPIRIDEACTIVE MOIETY6KY687524KGLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UGLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKGLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675GLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224
FERRIC OXIDE YELLOWINACTIVE INGREDIENTEX438O2MRTGLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XGLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30GLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224
POVIDONE K30INACTIVE INGREDIENTU725QWY32XGLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JGLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2GLIMEPIRIDE TABLET [MICRO LABS LIMITED]91224

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42571-103GLIMEPIRIDE (GLIMEPIRIDE) TABLET [MICRO LABS LIMITED]91233Current NDC, Legacy NDC, 2 package rows20250513_60e9397e-83b9-489e-9683-6f87e458bbaa.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199245glimepiride 1 MG Oral TabletPSN60e9397e-83b9-489e-9683-6f87e458bbaa91233
199246glimepiride 2 MG Oral TabletPSN60e9397e-83b9-489e-9683-6f87e458bbaa91233
153842glimepiride 3 MG Oral TabletPSN60e9397e-83b9-489e-9683-6f87e458bbaa91233
199247glimepiride 4 MG Oral TabletPSN60e9397e-83b9-489e-9683-6f87e458bbaa91233
1361493glimepiride 6 MG Oral TabletPSN60e9397e-83b9-489e-9683-6f87e458bbaa91233
1361495glimepiride 8 MG Oral TabletPSN60e9397e-83b9-489e-9683-6f87e458bbaa91233
199245glimepiride 1 MG Oral TabletSCD60e9397e-83b9-489e-9683-6f87e458bbaa91233
199246glimepiride 2 MG Oral TabletSCD60e9397e-83b9-489e-9683-6f87e458bbaa91233
153842glimepiride 3 MG Oral TabletSCD60e9397e-83b9-489e-9683-6f87e458bbaa91233
199247glimepiride 4 MG Oral TabletSCD60e9397e-83b9-489e-9683-6f87e458bbaa91233
1361493glimepiride 6 MG Oral TabletSCD60e9397e-83b9-489e-9683-6f87e458bbaa91233
1361495glimepiride 8 MG Oral TabletSCD60e9397e-83b9-489e-9683-6f87e458bbaa91233
199245glimepiride 1 MG Oral TabletPSN669a67c2-2f97-4b7e-8bba-83a015e0fa941
199246glimepiride 2 MG Oral TabletPSN669a67c2-2f97-4b7e-8bba-83a015e0fa941
199247glimepiride 4 MG Oral TabletPSN669a67c2-2f97-4b7e-8bba-83a015e0fa941
199245glimepiride 1 MG Oral TabletSCD669a67c2-2f97-4b7e-8bba-83a015e0fa941
199246glimepiride 2 MG Oral TabletSCD669a67c2-2f97-4b7e-8bba-83a015e0fa941
199247glimepiride 4 MG Oral TabletSCD669a67c2-2f97-4b7e-8bba-83a015e0fa941

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42571-103-0142571010301100 TABLET in 1 BOTTLE (42571-103-01) 100 tablet2013-06-130000-00-00NoNoCurrent
42571-103-0542571010305500 TABLET in 1 BOTTLE (42571-103-05) 500 tablet2013-06-130000-00-00NoNoCurrent