NDC 16729-002-17 - Glimepiride

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: 16729-002
Requested NDC: 16729-002-17
Package NDCs from labels: 16729-002-01, 16729-002-16, 16729-002-17
Manufacturer: Bryant Ranch Prepack
Effective date: 2026-05-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Glimepiride - Bryant Ranch Prepack	Bryant Ranch Prepack	2026-05-19	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - PD-Rx Pharmaceuticals, Inc.	PD-Rx Pharmaceuticals, Inc.	2026-01-07	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Northwind Health Company, LLC	Northwind Health Company, LLC	2026-01-01	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Accord Healthcare Inc \| Intas Pharmaceuticals Limited	Accord Healthcare Inc \| Intas Pharmaceuticals Limited	2025-10-17	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - REMEDYREPACK INC.	REMEDYREPACK INC.	2024-07-30	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Preferred Pharmaceuticals Inc.	Preferred Pharmaceuticals Inc.	2024-05-10	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - A-S Medication Solutions	A-S Medication Solutions	2023-02-28	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Proficient Rx LP	Proficient Rx LP	2022-10-01	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - NuCare Pharmaceuticals,Inc.	NuCare Pharmaceuticals,Inc.	2022-08-16	HUMAN PRESCRIPTION DRUG LABEL
GLIMEPIRIDE - Dircet_Rx	Dircet_Rx	2022-01-21	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - RedPharm Drug, Inc.	RedPharm Drug, Inc.	2022-01-20	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - NuCare Pharmaceuticals, Inc.	NuCare Pharmaceuticals, Inc.	2021-02-22	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Denton Pharma, Inc. DBA Northwind Pharmaceuticals	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	2021-01-14	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Denton Pharma, Inc. DBA Northwind Pharmaceuticals	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	2020-12-31	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Preferred Pharmaceuticals Inc.	Preferred Pharmaceuticals Inc.	2020-06-04	HUMAN PRESCRIPTION DRUG LABEL
GLIMEPIRIDE - Direct_Rx	Direct_Rx	2020-01-20	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Aidarex Pharmaceuticals LLC	Aidarex Pharmaceuticals LLC	2016-12-01	HUMAN PRESCRIPTION DRUG LABEL
GLIMEPIRIDE - DirectRX	DirectRX	2015-11-24	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
16729-002-01	Glimepiride	100 in 1 BOTTLE	TABLET	100	10
16729-002-16	Glimepiride	500 in 1 BOTTLE	TABLET	500	10
16729-002-17	Glimepiride	1000 in 1 BOTTLE	TABLET	1000	10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
16729-002	GLIMEPIRIDE TABLET [ACCORD HEALTHCARE INC]	9	Current NDC, Legacy NDC, 3 package rows	20231129_9b74fbac-9e04-4927-9981-1e3dace89c6d.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
16729-002-01	EA - Each	16729-002	08a03fc2-8f33-47f5-b9d8-86517569fcf2	1	2012-07-24
16729-002-16	EA - Each	16729-002	e1715c83-c25a-4200-90ec-893cd01df508	1	2016-10-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
GLIMEPIRIDE	ACTIVE INGREDIENT	6KY687524K	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	7
GLIMEPIRIDE	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	7
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	7
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	7
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	7
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	7
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	7
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	7
GLIMEPIRIDE	ACTIVE INGREDIENT	6KY687524K	GLIMEPIRIDE TABLET [ACCORD HEALTHCARE INC]	4
GLIMEPIRIDE	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE TABLET [ACCORD HEALTHCARE INC]	4
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	GLIMEPIRIDE TABLET [ACCORD HEALTHCARE INC]	4
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	GLIMEPIRIDE TABLET [ACCORD HEALTHCARE INC]	4
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	GLIMEPIRIDE TABLET [ACCORD HEALTHCARE INC]	4
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	GLIMEPIRIDE TABLET [ACCORD HEALTHCARE INC]	4
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	GLIMEPIRIDE TABLET [ACCORD HEALTHCARE INC]	4
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	GLIMEPIRIDE TABLET [ACCORD HEALTHCARE INC]	4
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	GLIMEPIRIDE TABLET [ACCORD HEALTHCARE INC]	4
GLIMEPIRIDE	ACTIVE INGREDIENT	6KY687524K	GLIMEPIRIDE TABLET [DIRECTRX]	1
GLIMEPIRIDE	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE TABLET [DIRECTRX]	1
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	GLIMEPIRIDE TABLET [DIRECTRX]	1
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	GLIMEPIRIDE TABLET [DIRECTRX]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	GLIMEPIRIDE TABLET [DIRECTRX]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	GLIMEPIRIDE TABLET [DIRECTRX]	1
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	GLIMEPIRIDE TABLET [DIRECTRX]	1
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	GLIMEPIRIDE TABLET [DIRECTRX]	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 7 of 11 · 205 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Calamine Plus Pramoxine HCl	CALAMINE PLUS SPRAY	FSA Store Inc.	3cd18f96-34f7-3f2c-e063-6294a90a3b7e	2025-08-19	Warnings	Exact identifier unii: 1K09F3G675
Glimepiride	GLIMEPIRIDE	A-S Medication Solutions	489dc098-0ac7-4f8e-b258-326229539c7c	2025-08-15	Warnings, Adverse reactions	Exact identifier rxcui: 199246 unii: 6KY687524K
Glimepiride	GLIMEPIRIDE	A-S Medication Solutions	be7175ae-ba53-45b8-9554-e4f4ebf56883	2025-08-15	Warnings, Adverse reactions	Exact identifier rxcui: 199246 unii: 6KY687524K
1f36b65a-f1d7-4bf2-bfcd-713b926774c0			dac7b655-d2e3-458a-9a8d-677757ba2a75	2025-07-23	Warnings, Adverse reactions	Exact identifier spl set id: dac7b655-d2e3-458a-9a8d-677757ba2a75
Glimepiride	GLIMEPIRIDE	BluePoint Laboratories	a01b0466-13f5-4c47-ae55-c5f1527d9414	2025-07-07	Warnings, Adverse reactions	Exact identifier rxcui: 199247 rxcui: 199245 rxcui: 199246 unii: 6KY687524K
Ferrum rosatum Graphites	FERRUM ROSATUM GRAPHITES	Uriel Pharmacy Inc.	1a4ca338-eada-4c0f-8bce-480244940c89	2025-06-27	Warnings	Exact identifier unii: 1K09F3G675
Glimepiride	GLIMEPIRIDE	Bryant Ranch Prepack	d4513181-4558-4d9a-851b-acf7e3eda25a	2025-06-16	Warnings, Adverse reactions	Exact identifier rxcui: 199245 unii: 6KY687524K
a0a4f5a0-b86c-4f4d-ac8a-b1ca8a7d4c67			8ba135eb-bfb4-4cc2-a8c9-8f750ca3e807	2025-06-13	Warnings, Adverse reactions	Exact identifier spl set id: 8ba135eb-bfb4-4cc2-a8c9-8f750ca3e807
Aquavit	AQUAVIT	Uriel Pharmacy Inc.	c1c0887a-c388-c737-e053-2a95a90a076c	2025-06-06	Warnings	Exact identifier unii: 1K09F3G675
Glimepiride	GLIMEPIRIDE	ST. MARY'S MEDICAL PARK PHARMACY	35ba31ef-2b90-61c6-e063-6394a90a59ee	2025-05-22	Warnings, Adverse reactions	Exact identifier rxcui: 199247 unii: 6KY687524K
Glimepiride	GLIMEPIRIDE	Micro Labs Limited	60e9397e-83b9-489e-9683-6f87e458bbaa	2025-05-12	Warnings, Adverse reactions	Exact identifier rxcui: 199247 rxcui: 199245 rxcui: 199246 unii: 6KY687524K
Powder	TITANIUM DIOXIDE	Oxygen Development LLC	08b7eeeb-09ae-ffe6-e063-6294a90aba90	2025-05-07	Warnings	Exact identifier unii: 1K09F3G675
Glimepiride	GLIMEPIRIDE	A-S Medication Solutions	49bf2d48-efa8-487b-b861-0124c3a4c951	2025-04-01	Warnings, Adverse reactions	Exact identifier rxcui: 199245 unii: 6KY687524K
Duetact	PIOGLITAZONE AND GLIMEPIRIDE	Takeda Pharmaceuticals America, Inc.	f8b0c917-3fdd-4a28-a47d-6225b8195458	2025-03-27	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 6KY687524K
RID Poison Ivy Rash Relief	CALAMINE AND ZINC OXIDE	Oystershell Consumer Health Inc.	36c3af9a-2646-4427-e063-6394a90a2c5e	2025-03-13	Warnings	Exact identifier unii: 1K09F3G675
Walgreens Soothing Eye Relief Lubricant Eye Drops	POLYVINYL ALCOHOL, POVIDONE	Walgreens Co.	29b7387b-ad65-3a11-e063-6394a90a6a15	2025-02-14	Warnings	Exact identifier unii: FZ989GH94E
Calamine	FERRIC OXIDE RED	Preferred Pharmaceuticals Inc.	326f3d80-c1bf-4cf0-a662-58e02ed7ee67	2025-02-12	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Glimepiride	GLIMEPIRIDE	Bryant Ranch Prepack	661b5b13-6334-4965-8dc5-709e19080584	2025-01-28	Warnings, Adverse reactions	Exact identifier rxcui: 199245 unii: 6KY687524K
Glimepiride	GLIMEPIRIDE	Direct_Rx	fd26934e-daea-f47b-e053-6394a90a4bc6	2025-01-22	Warnings, Adverse reactions	Exact identifier rxcui: 199246 unii: 6KY687524K
Prunus Iron	PRUNUS IRON	Uriel Pharmacy Inc.	091be588-b62e-4919-8e9e-3edb9792d319	2025-01-22	Warnings	Exact identifier unii: 1K09F3G675

Reported adverse events (FAERS/openFDA)#

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