NDC 16729-003-17 - 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: 16729-003
Requested NDC: 16729-003-17
Package NDCs from labels: 16729-003-01, 16729-003-16, 16729-003-17
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.	2025-03-25	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 - DIRECT RX	DIRECT RX	2023-01-11	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - St. Mary’s Medical Park Pharmacy	St. Mary’s Medical Park Pharmacy	2022-12-22	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - REMEDYREPACK INC.	REMEDYREPACK INC.	2022-06-09	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Proficient Rx LP	Proficient Rx LP	2022-04-01	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - RedPharm Drug, Inc.	RedPharm Drug, Inc.	2022-01-20	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Quality Care Products, LLC	Quality Care Products, LLC	2021-04-14	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - NuCare Pharmaceuticals, Inc.	NuCare Pharmaceuticals, Inc.	2021-02-23	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - NuCare Pharmaceuticals,Inc.	NuCare Pharmaceuticals,Inc.	2021-02-18	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Denton Pharma, Inc. DBA Northwind Pharmaceuticals	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	2020-12-30	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Denton Pharma, Inc. dba Northwind Pharmaceuticals	Denton Pharma, Inc. dba Northwind Pharmaceuticals	2020-09-15	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Preferred Pharmaceuticals Inc.	Preferred Pharmaceuticals Inc.	2018-06-18	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
16729-003-01	Glimepiride	100 in 1 BOTTLE	TABLET	100	10
16729-003-16	Glimepiride	500 in 1 BOTTLE	TABLET	500	10
16729-003-17	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
16729-003	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
16729-003-01	EA - Each	16729-003	0076d1ca-2a13-4bfb-98ee-17258bd8f77a	1	2013-02-13
16729-003-16	EA - Each	16729-003	f401dc9e-e474-41a4-b426-cd34551a4dc8	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.]	5
GLIMEPIRIDE	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	5
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	5
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	5
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	5
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	5
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	GLIMEPIRIDE TABLET [PD-RX PHARMACEUTICALS, INC.]	5
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 [PROFICIENT RX LP]	1
GLIMEPIRIDE	ACTIVE INGREDIENT	6KY687524K	GLIMEPIRIDE TABLET [NORTHWIND PHARMACEUTICALS]	1
GLIMEPIRIDE	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE TABLET [NORTHWIND PHARMACEUTICALS]	1
glimepiride	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE TABLET [PROFICIENT RX LP]	1
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	GLIMEPIRIDE TABLET [PROFICIENT RX LP]	1
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	GLIMEPIRIDE TABLET [PROFICIENT RX LP]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	GLIMEPIRIDE TABLET [PROFICIENT RX LP]	1
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	GLIMEPIRIDE TABLET [PROFICIENT RX LP]	1
sodium starch glycolate type a potato	INACTIVE INGREDIENT	5856J3G2A2	GLIMEPIRIDE TABLET [PROFICIENT RX LP]	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 3 of 11 · 206 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Glimepiride	GLIMEPIRIDE	Bryant Ranch Prepack	62780d2e-083d-4bcb-99ff-1b1b4ade60d9	2026-03-09	Warnings, Adverse reactions	Exact identifier rxcui: 199246 unii: 6KY687524K
Calamine	CALAMINE, PRAMOXINE HCL	Amazon.com Services LLC	aceb0b10-8c90-4a06-8c47-cd1a2b4676a3	2026-03-03	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	FERRIC OXIDE RED	Old East Main Co.	c38c77fd-abbf-4c87-a9c0-a0e21ed3f97d	2026-03-02	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	FERRIC OXIDE RED	Chain Drug Marketing Association	86ff4875-9007-4b7b-8f46-16cbd475d4bb	2026-02-27	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	CALAMINE, PRAMOXINE HCL	Chain Drug Marketing Association	6c848b98-f01c-40f2-a9aa-2af76cb370c8	2026-02-27	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Levico Prunus	LEVICO PRUNUS	Uriel Pharmacy Inc.	63db9374-8ee2-48cf-8799-454c95869808	2026-02-27	Warnings	Exact identifier unii: 1K09F3G675
Glimepiride	GLIMEPIRIDE	PD-Rx Pharmaceuticals, Inc.	1450f455-a14a-4f9b-b3aa-dae49ea0c186	2026-02-26	Warnings, Adverse reactions	Exact identifier rxcui: 199246 unii: 6KY687524K
Calamine	FERRIC OXIDE RED	Family Dollar Stores, Inc	1a03331e-3676-451c-be22-9a547e8ae6e2	2026-02-24	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	FERRIC OXIDE RED	Perrigo Direct, Inc	256bd1d4-fd50-408f-9aee-84f218bb4971	2026-02-19	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Glimepiride	GLIMEPIRIDE	NuCare Pharmaceuticals,Inc.	bf8e5993-5ee7-d26d-e053-2a95a90ae5df	2026-02-19	Warnings, Adverse reactions	Exact identifier rxcui: 199246 unii: 6KY687524K
Calamine	CALAMINE, PRAMOXIND HCL	Perrigo Direct, Inc	54a20ec9-ab86-4410-af94-e04393e9d4b3	2026-02-19	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	CALAMINE, PRAMOXINE HCL	Meijer, Inc.	6b369ef2-fd54-4931-a9eb-0fb42834c2ef	2026-02-19	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	FERRIC OXIDE RED	Target Corporation	d4ee05c8-ae62-45df-8783-1ed57fa030ec	2026-02-18	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	FERRIC OXIDE RED	Topco Associates LLC	2b32e720-ac71-4d60-bc06-e28a00f8a450	2026-02-13	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Calamine	CALAMINE, PRAMOXINE HCL	Topco Associates LLC	15d1ae3f-509c-4e6b-8f0c-cf9265680358	2026-02-13	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
GoodSense Eye Drops Advanced Relief Moisturizer	DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL	Sportpharm LLC	8d58dcbb-72a0-41f0-9eeb-613072a6d7ae	2026-02-06	Warnings	Exact identifier unii: FZ989GH94E
Calamine	FERRIC OXIDE RED	Major Pharmaceuticals	c25be68d-834a-4959-8d47-01ec789406ba	2026-02-04	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
MINIDROPS	LUBRICANT EYE DROPS	Optics Laboratory, Inc	c13c5f91-50df-471c-a7c9-1747a2ac1250	2026-02-03	Warnings	Exact identifier unii: FZ989GH94E
Aquavit 1	AQUAVIT 1	Uriel Pharmacy Inc.	2354fcfc-05a2-444a-ace4-b3df61413157	2026-02-02	Warnings	Exact identifier unii: 1K09F3G675
Glimepiride	GLIMEPIRIDE	Proficient Rx LP	dbed06f9-7758-4c96-9af0-1ed6103db7df	2026-02-01	Warnings, Adverse reactions	Exact identifier rxcui: 199246 unii: 6KY687524K

Reported adverse events (FAERS/openFDA)#

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