NDC 60505-0145-02 - Omeprazole

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: 60505-0145
Requested NDC: 60505-0145-02
Package NDCs from labels: 60505-0145-0, 60505-0145-2, 60505-0145-1, 60505-0145-3, 60505-0145-7, 60505-0145-02
Manufacturer: Proficient Rx LP
Effective date: 2024-10-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Omeprazole - Proficient Rx LP	Proficient Rx LP	2024-10-01	HUMAN PRESCRIPTION DRUG LABEL
Omeprazole - Apotex Corp \| Apotex Inc.	Apotex Corp \| Apotex Inc.	2024-04-22	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
60505-0145-0	Omeprazole	30 in 1 BOTTLE	CAPSULE, DELAYED RELEASE	30	35
60505-0145-1	Omeprazole	1000 in 1 BOTTLE	CAPSULE, DELAYED RELEASE	1000	35
60505-0145-2	Omeprazole	100 in 1 BOTTLE	CAPSULE, DELAYED RELEASE	100	35
60505-0145-3	Omeprazole	7 in 1 CARTON	CAPSULE, DELAYED RELEASE	7	35
60505-0145-3	Omeprazole	10 in 1 BLISTER PACK	CAPSULE, DELAYED RELEASE	10	35
60505-0145-7	Omeprazole	10 in 1 CARTON	CAPSULE, DELAYED RELEASE	10	35
60505-0145-7	Omeprazole	10 in 1 BLISTER PACK	CAPSULE, DELAYED RELEASE	10	35

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
60505-0145	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	35	Current NDC, Legacy NDC, 7 package rows	20240423_b83329ac-a65e-b3af-a3fb-c5a6c740e5e7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
60505-0145-0	EA - Each	60505-0145	75ce3b5d-8269-41ec-9c0f-023d1757c956	1	2012-07-24
60505-0145-1	EA - Each	60505-0145	9d84a9fb-3618-4057-98fe-763f7bfa48b3	1	2012-07-24
60505-0145-2	EA - Each	60505-0145	31a33844-de11-4a38-aef8-e675081b4075	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Omeprazole	ACTIVE INGREDIENT	KG60484QX9	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
Omeprazole	ACTIVE MOIETY	KG60484QX9	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
AMMONIA	INACTIVE INGREDIENT	5138Q19F1X	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
BUTYL ALCOHOL	INACTIVE INGREDIENT	8PJ61P6TS3	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
GELATIN	INACTIVE INGREDIENT	2G86QN327L	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
MAGNESIUM HYDROXIDE	INACTIVE INGREDIENT	NBZ3QY004S	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
POTASSIUM HYDROXIDE	INACTIVE INGREDIENT	WZH3C48M4T	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
POVIDONE K30	INACTIVE INGREDIENT	U725QWY32X	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
SHELLAC	INACTIVE INGREDIENT	46N107B71O	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	OMEPRAZOLE CAPSULE, DELAYED RELEASE [APOTEX CORP]	15
OMEPRAZOLE	ACTIVE INGREDIENT	KG60484QX9	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
Omeprazole	ACTIVE MOIETY	KG60484QX9	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
AMMONIA	INACTIVE INGREDIENT	5138Q19F1X	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
BUTYL ALCOHOL	INACTIVE INGREDIENT	8PJ61P6TS3	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
GELATIN	INACTIVE INGREDIENT	2G86QN327L	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
MAGNESIUM HYDROXIDE	INACTIVE INGREDIENT	NBZ3QY004S	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
POTASSIUM HYDROXIDE	INACTIVE INGREDIENT	WZH3C48M4T	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
POVIDONE K30	INACTIVE INGREDIENT	U725QWY32X	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
SHELLAC	INACTIVE INGREDIENT	46N107B71O	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	OMEPRAZOLE CAPSULE, DELAYED RELEASE [PROFICIENT RX LP]	3

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 1 of 310 · 6,184 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
hand sanitizer chocolate chip cookie scent	ETHYL ALCOHOL	Diamond Life Cosmetics Trading FZCO	69d423f2-ff9f-48e0-a553-c7f4aaf37b29	2026-09-17	Warnings	Exact identifier unii: 3K9958V90M
Stay Ageless Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	W Aesthetics	5b0f2c8f-d6fa-5e25-e063-6394a90a084d	2026-09-09	Warnings	Exact identifier unii: 15FIX9V2JP
Advanced Alcohol Gel Sanitizer	ALCOHOL	Betco Corporation, Ltd	a23b997c-b010-5985-e053-2995a90aadf3	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
Touchland Power Mist Hydrating Hand Sanitizer Cotton Candy	ALCOHOL	Church & Dwight Co., Inc.	5b107dd2-a76c-9c80-e063-6394a90aaedb	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
Pink Touchland Power Mist Hydrating Hand Sanitizer Wild Watermelon	ALCOHOL	Church & Dwight Co., Inc.	5b108f13-6474-fdbd-e063-6294a90a1a2b	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
Touchland Power Mist Hydrating Hand Sanitizer Mango Passion	ALCOHOL	Church & Dwight Co., Inc.	5b1099ae-f1e8-b79d-e063-6394a90add6f	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
Touchland Gentle Mist Hand Sanitizer Lily of The Valley	ALCOHOL	Church & Dwight Co., Inc.	5b10a3a7-1cca-2a34-e063-6294a90a3f6c	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
Touchland Glow Mist Hand Sanitizer Rosewater	ALCOHOL	Church & Dwight Co., Inc.	5a850866-bc5d-e595-e063-6394a90a335f	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
COMPLETE ACID REDUCER	FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	b023cd92-eabb-474b-9b5a-4b46cf48256b	2026-09-08	Warnings	Exact identifier unii: NBZ3QY004S
Alcohol Prep Pad Medium	ALCOHOL PREP PAD	Yangzhou Huanrui Medical Technology Co., Ltd	5af3eedc-d01e-c9e9-e063-6394a90a49e1	2026-09-08	Warnings	Exact identifier unii: ND2M416302
Verifine	ALCOHOL SWABS	Promisemed Hangzhou Meditech Co., LTD	5af9f31b-0c92-e3a9-e063-6394a90a38c9	2026-09-08	Warnings	Exact identifier unii: ND2M416302
Verifine	ALCOHOL SWABS	Promisemed Hangzhou Meditech Co., LTD	5afc0201-490e-ccf3-e063-6394a90aadad	2026-09-08	Warnings	Exact identifier unii: ND2M416302
Sting Relief Pad	BENZOCAINE, ISOPROPYL ALCOHOL CLOTH	JINHUA JINGDI MEDICAL SUPPLIES CO., LTD	57ccc28b-5f5f-30ec-e063-6294a90a081c	2026-09-07	Warnings	Exact identifier unii: ND2M416302
hand sanitizer - cherry sundae	ALCOHOL	Ganzhou Olivee Cosmetic Co., Ltd.	270d2ce0-6310-4a84-be8a-72db6062bae7	2026-09-07	Warnings	Exact identifier unii: 3K9958V90M
hand sanitizer - vanilla frosting	ALCOHOL	Ganzhou Olivee Cosmetic Co., Ltd.	f6cabda2-6e1c-4238-9a2e-df10e263517d	2026-09-07	Warnings	Exact identifier unii: 3K9958V90M
hydrating mist hand sanitizer with silicone keychain holder - beaver nuggets	ALCOHOL	Ganzhou Olivee Cosmetic Co., Ltd.	ba3612b3-9696-417a-ba66-eb9dc5ea27c6	2026-09-07	Warnings	Exact identifier unii: 3K9958V90M
hydrating mist hand sanitizer with silicone keychain holder - signature scent	ALCOHOL	Ganzhou Olivee Cosmetic Co., Ltd.	5b0ac694-66e0-437f-86cd-09f259344b89	2026-09-07	Warnings	Exact identifier unii: 3K9958V90M
ALCOHOL PREP PADS MEDIUM STERILE	ISOPROPYL ALCOHOL CLOTH	JINHUA JINGDI MEDICAL SUPPLIES CO., LTD	57cbbe72-24ec-2e4a-e063-6394a90abbd2	2026-09-07	Warnings	Exact identifier unii: ND2M416302
Sweethearts - Crush On You - Peach Skin	ALCOHOL	Scent Theory Products LLC	5ac32582-d888-edf4-e063-6394a90a40ab	2026-09-05	Warnings	Exact identifier unii: 3K9958V90M
Sweethearts - Be Mine - Sugared Berries	ALCOHOL	Scent Theory Products LLC	5ac32ffb-926a-f249-e063-6394a90a8d87	2026-09-05	Warnings	Exact identifier unii: 3K9958V90M

Reported adverse events (FAERS/openFDA)#

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