NDC 55111-320-79 - 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: 55111-320
Requested NDC: 55111-320-79
Package NDCs from labels: 55111-320-30, 55111-320-01, 55111-320-05, 55111-320-79, 55111-320-78
Manufacturer: AvPAK
Effective date: 2026-01-14
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Glimepiride - AvPAK	AvPAK	2026-01-14	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - PD-Rx Pharmaceuticals, Inc.	PD-Rx Pharmaceuticals, Inc.	2025-10-15	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - American Health Packaging	American Health Packaging	2024-11-13	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Proficient Rx LP	Proficient Rx LP	2024-09-01	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - REMEDYREPACK INC.	REMEDYREPACK INC.	2024-03-27	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Bryant Ranch Prepack	Bryant Ranch Prepack	2021-12-21	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Bryant Ranch Prepack	Bryant Ranch Prepack	2021-11-22	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride	Dr. Reddy's Laboratories Limited \| Dr. Reddy's Laboratories Limited (FTO-III) \| DR. REDDY'S LABORATORIES LIMITED (FTO-Sez-Process Unit-01)	2019-01-16	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - NCS HealthCare of KY, Inc dba Vangard Labs	NCS HealthCare of KY, Inc dba Vangard Labs	2013-08-26	HUMAN PRESCRIPTION DRUG LABEL
Glimepiride - Rebel Distributors Corp	Rebel Distributors Corp	2010-09-28	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
55111-320-01	Glimepiride	100 in 1 BOTTLE	TABLET	100	12
55111-320-05	Glimepiride	500 in 1 BOTTLE	TABLET	500	12
55111-320-30	Glimepiride	30 in 1 BOTTLE	TABLET	30	12
55111-320-78	Glimepiride	100 in 1 CARTON	TABLET	100	12
55111-320-79	Glimepiride	1 in 1 BLISTER PACK	TABLET	1	12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55111-320	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	12	Current NDC, Legacy NDC, 5 package rows	20190130_07ad4366-4b21-f633-49f3-c2b35f88168d.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
55111-320-01	EA - Each	55111-320	107e9e7b-88fa-4288-9932-960958715310	1	2012-07-24
55111-320-05	EA - Each	55111-320	518a4018-d2c6-4f2d-8e37-3f31a0d2cac8	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
GLIMEPIRIDE	ACTIVE INGREDIENT	6KY687524K	GLIMEPIRIDE TABLET [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	10
GLIMEPIRIDE	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE TABLET [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	10
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	GLIMEPIRIDE TABLET [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	10
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	GLIMEPIRIDE TABLET [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	10
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	GLIMEPIRIDE TABLET [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	10
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	GLIMEPIRIDE TABLET [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	10
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	GLIMEPIRIDE TABLET [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	10
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	GLIMEPIRIDE TABLET [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	10
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	GLIMEPIRIDE TABLET [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	10
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	GLIMEPIRIDE TABLET [NCS HEALTHCARE OF KY, INC DBA VANGARD LABS]	10
GLIMEPIRIDE	ACTIVE INGREDIENT	6KY687524K	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	7
GLIMEPIRIDE	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	7
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	7
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	7
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	7
ferric oxide red	INACTIVE INGREDIENT	1K09F3G675	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	7
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	7
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	7
Povidone	INACTIVE INGREDIENT	FZ989GH94E	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	7
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	GLIMEPIRIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]	7
GLIMEPIRIDE	ACTIVE INGREDIENT	6KY687524K	GLIMEPIRIDE TABLET [AMERICAN HEALTH PACKAGING]	3
GLIMEPIRIDE	ACTIVE INGREDIENT	6KY687524K	GLIMEPIRIDE (GLIMEPIRIDE ) TABLET [PD-RX PHARMACEUTICALS, INC.]	3
GLIMEPIRIDE	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE TABLET [AMERICAN HEALTH PACKAGING]	3
GLIMEPIRIDE	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE (GLIMEPIRIDE ) TABLET [PD-RX PHARMACEUTICALS, INC.]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	GLIMEPIRIDE TABLET [AMERICAN HEALTH PACKAGING]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	GLIMEPIRIDE (GLIMEPIRIDE ) TABLET [PD-RX PHARMACEUTICALS, INC.]	3
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	GLIMEPIRIDE TABLET [AMERICAN HEALTH PACKAGING]	3
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	GLIMEPIRIDE TABLET [AMERICAN HEALTH PACKAGING]	3
ferric oxide red	INACTIVE INGREDIENT	1K09F3G675	GLIMEPIRIDE (GLIMEPIRIDE ) TABLET [PD-RX PHARMACEUTICALS, INC.]	3
ferric oxide red	INACTIVE INGREDIENT	1K09F3G675	GLIMEPIRIDE TABLET [AMERICAN HEALTH PACKAGING]	3
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	GLIMEPIRIDE (GLIMEPIRIDE ) TABLET [PD-RX PHARMACEUTICALS, INC.]	3
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	GLIMEPIRIDE TABLET [AMERICAN HEALTH PACKAGING]	3
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	GLIMEPIRIDE (GLIMEPIRIDE ) TABLET [PD-RX PHARMACEUTICALS, INC.]	3
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	GLIMEPIRIDE TABLET [AMERICAN HEALTH PACKAGING]	3
povidone	INACTIVE INGREDIENT	FZ989GH94E	GLIMEPIRIDE (GLIMEPIRIDE ) TABLET [PD-RX PHARMACEUTICALS, INC.]	3
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	GLIMEPIRIDE TABLET [AMERICAN HEALTH PACKAGING]	3
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	GLIMEPIRIDE (GLIMEPIRIDE ) TABLET [PD-RX PHARMACEUTICALS, INC.]	3
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	GLIMEPIRIDE TABLET [AMERICAN HEALTH PACKAGING]	3
GLIMEPIRIDE	ACTIVE INGREDIENT	6KY687524K	GLIMEPIRIDE TABLET [REBEL DISTRIBUTORS CORP]	2
GLIMEPIRIDE	ACTIVE MOIETY	6KY687524K	GLIMEPIRIDE TABLET [REBEL DISTRIBUTORS CORP]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	GLIMEPIRIDE TABLET [REBEL DISTRIBUTORS CORP]	2
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	GLIMEPIRIDE TABLET [REBEL DISTRIBUTORS CORP]	2
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	GLIMEPIRIDE TABLET [REBEL DISTRIBUTORS CORP]	2
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	GLIMEPIRIDE TABLET [REBEL DISTRIBUTORS CORP]	2
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	GLIMEPIRIDE TABLET [REBEL DISTRIBUTORS CORP]	2
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	GLIMEPIRIDE TABLET [REBEL DISTRIBUTORS CORP]	2
povidone	INACTIVE INGREDIENT	FZ989GH94E	GLIMEPIRIDE TABLET [REBEL DISTRIBUTORS CORP]	2
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	GLIMEPIRIDE TABLET [REBEL DISTRIBUTORS CORP]	2

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 6 of 11 · 202 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	HY-VEE, INC	415ecfe9-3145-f23e-e063-6394a90adfd8	2025-11-17	Warnings	Exact identifier unii: 1K09F3G675
Au Kah Chuen Fugical	CALAMINE AND DIPHENHYDRAMINE HYDROCHLORID	Zhejiang Dingtai Pharmaceutical Co., Ltd	5b4add17-6c3d-4093-826a-2edb41c1d1db	2025-11-10	Warnings	Exact identifier unii: 1K09F3G675
FARGELIN HEMORRHOIDAL	CALAMINE, PETROLATUM AND PHENYLEPHRINE HYDROCHLORIDE	MADISON ONE ACME INC	6844ad63-512d-496a-9458-011894185b0d	2025-11-10	Warnings	Exact identifier unii: 1K09F3G675
Calamine Plus	CALAMINE PLUS PRAMOXINE HCL	Chain Drug Marketing Association Inc	1a3f8819-58cf-8923-e063-6394a90a37af	2025-11-06	Warnings	Exact identifier unii: 1K09F3G675
Calamine Plus Pramoxine HCl	CALAMINE PLUS NO TOUCH SPRAY	Premier Brands of America Inc.	36481d67-2346-470b-e063-6294a90aae99	2025-11-03	Warnings	Exact identifier unii: 1K09F3G675
Calamine Plus	CALAMINE PLUS PRAMOXINE HCL	AmerisourceBergen Drug Corporation	f161e151-4fab-2fbc-e053-2a95a90a5437	2025-10-30	Warnings	Exact identifier unii: 1K09F3G675
REMEDY Calazime Skin Protectant	CALAMINE, MENTHOL, WHITE PETROLATUM, ZINC OXIDE	Medline Industries, LP	1295cfcc-5b61-481b-964b-f53ffd0cb58e	2025-10-30	Warnings	Exact identifier unii: 1K09F3G675
Calamine Plus	CALAMINE PLUS PRAMOXINE HCL	Meijer Distribution Inc.	03c46823-0b1f-4101-e063-6294a90aaf94	2025-10-30	Warnings	Exact identifier unii: 1K09F3G675
Aveeno Anti-Itch Concentrated	ZINC OXIDE, FERRIC OXIDE RED, AND PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	07f4d4d0-9cee-46c3-bc71-2024abd31c9e	2025-10-29	Warnings	Exact identifier unii: 1K09F3G675
LACRIFRESH HYDRAPF	GLYCERIN, POVIDONE	AVIZOR, S.A.	41bbd23e-0ec8-eb18-e063-6294a90a46d1	2025-10-27	Warnings	Exact identifier unii: FZ989GH94E
LACRIFRESH HYDRAMAXPF	GLYCERIN, POVIDONE	AVIZOR, S.A.	41be1604-89b4-7ec3-e063-6294a90a3331	2025-10-27	Warnings	Exact identifier unii: FZ989GH94E
Calamine Plus Pramoxine HCl	CALAMINE PLUS SPRAY	Premier Brands of America, Inc.	d3452573-f91f-f157-e053-2a95a90a1ad8	2025-10-27	Warnings	Exact identifier unii: 1K09F3G675
Stye	POLYVINYL ALCOHOL AND POVIDONE	Medtech Products Inc.	60c11d3d-df20-4d1c-b425-49a84fecea30	2025-10-23	Warnings	Exact identifier unii: FZ989GH94E
iVIZIA Dry Eye	POVIDONE	Thea Pharma Inc.	1ef73cb1-da48-a713-e063-6294a90afa9d	2025-10-20	Warnings	Exact identifier unii: FZ989GH94E
Glimepiride	GLIMEPIRIDE	Accord Healthcare Inc	9b74fbac-9e04-4927-9981-1e3dace89c6d	2025-10-17	Warnings, Adverse reactions	Exact identifier rxcui: 199247 rxcui: 199245 rxcui: 199246 unii: 6KY687524K
Glimepiride	GLIMEPIRIDE	PD-Rx Pharmaceuticals, Inc.	101cdc41-2131-4425-b550-6a0a60b5f4a4	2025-10-15	Warnings, Adverse reactions	Exact identifier application number: ANDA077091 rxcui: 199247 unii: 6KY687524K
Glimepiride	GLIMEPIRIDE	PD-Rx Pharmaceuticals, Inc.	657f1b51-2f82-44f6-a23d-97f4b34b3c45	2025-10-15	Warnings, Adverse reactions	Exact identifier application number: ANDA077091 ndc (package): 43063-121-30 ndc (package): 43063-121-90 ndc (product): 43063-121 rxcui: 199245 spl id: 4137398e-13df-7c18-e063-6394a90ac45d spl set id: 657f1b51-2f82-44f6-a23d-97f4b34b3c45 unii: 6KY687524K
Eyes Irritation Relief	POLYVINYL ALCOHOL AND POVIDONE AND TETRAHYDROZOLINE HYDROCHLORIDE	CARDINAL HEALTH 110, LLC. DBA LEADER	bd2608c6-ffdf-352a-e053-2995a90a26a8	2025-09-12	Warnings	Exact identifier unii: FZ989GH94E
Powder	TITANIUM DIOXIDE	Oxygen Development LLC	08b52f29-c1a0-c673-e063-6294a90a9a7a	2025-09-05	Warnings	Exact identifier unii: 1K09F3G675
Powder	TITANIUM DIOXIDE	Oxygen Development LLC	08b8003f-40be-3380-e063-6294a90a4f6b	2025-09-05	Warnings	Exact identifier unii: 1K09F3G675

Reported adverse events (FAERS/openFDA)#

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