NDC 0641-6006-01 - Atropine Sulfate

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: 0641-6006
Requested NDC: 0641-6006-01
Package NDCs from labels: 0641-6006-01, 0641-6006-10
Manufacturer: Hikma Pharmaceuticals USA Inc.
Effective date: 2024-04-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Atropine Sulfate Injection, USP	Hikma Pharmaceuticals USA Inc.	2024-04-08	HUMAN PRESCRIPTION DRUG LABEL
Atropine Sulfate - Medical Purchasing Solutions, LLC	Medical Purchasing Solutions, LLC	2023-05-31	HUMAN PRESCRIPTION DRUG LABEL
Atropine Sulfate - General Injectables & Vaccines, Inc	General Injectables & Vaccines, Inc	2022-12-09	HUMAN PRESCRIPTION DRUG LABEL
Atropine Sulfate Injection, USP FOR IM, IV, OR SC USE Rx Only	Henry Schein, Inc.	2022-01-09	HUMAN PRESCRIPTION DRUG LABEL
ATROPINE SULFATE - HF Acquisition Co LLC, DBA HealthFirst	HF Acquisition Co LLC, DBA HealthFirst	2020-09-04	HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2012-07-24	Indexing - Billing Unit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0641-6006-01	Atropine Sulfate	20 mL in 1 VIAL	INJECTION	20		4
0641-6006-10	Atropine Sulfate	10 in 1 CARTON	INJECTION	10		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0641-6006	ATROPINE SULFATE INJECTION [HIKMA PHARMACEUTICALS USA INC.]	4	Legacy NDC, 2 package rows	20240410_5d45eb2f-b964-4f64-b277-eef807520466.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0641-6006-01	ML - Milliliter	0641-6006	0dd1cebf-afb5-463c-8066-2ae1248537db	1	2012-07-24
0641-6006-10	ML - Milliliter	0641-6006	50fad021-aa7f-43ab-b295-6c10da590ef3	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ATROPINE SULFATE	ACTIVE INGREDIENT	03J5ZE7KA5	ATROPINE SULFATE INJECTION [WEST-WARD PHARMACEUTICAL CORP.]	1
Atropine Sulfate	ACTIVE INGREDIENT	03J5ZE7KA5	ATROPINE SULFATE INJECTION [GENERAL INJECTABLES & VACCINES, INC]	1
ATROPINE	ACTIVE MOIETY	7C0697DR9I	ATROPINE SULFATE INJECTION [WEST-WARD PHARMACEUTICAL CORP.]	1
Atropine	ACTIVE MOIETY	7C0697DR9I	ATROPINE SULFATE INJECTION [GENERAL INJECTABLES & VACCINES, INC]	1
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	ATROPINE SULFATE INJECTION [WEST-WARD PHARMACEUTICAL CORP.]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	ATROPINE SULFATE INJECTION [WEST-WARD PHARMACEUTICAL CORP.]	1
SULFURIC ACID	INACTIVE INGREDIENT	O40UQP6WCF	ATROPINE SULFATE INJECTION [WEST-WARD PHARMACEUTICAL CORP.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ATROPINE SULFATE INJECTION [WEST-WARD PHARMACEUTICAL CORP.]	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 20 of 61 · 1,220 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eyesaline Emergency Eyewash	PURIFIED WATER	Honeywell Safety Products USA, Inc.	37f244fd-c02f-e66a-e063-6394a90aed81	2025-11-12	Warnings	Exact identifier unii: 059QF0KO0R
SODIUM CHLORIDE	SODIUM CHLORIDE	Hospira, Inc.	af6aebad-ef03-4d19-9a40-18e5a278b812	2025-11-11	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
GURUNANDA NASAL SALINE	NASAL WASH	GURUNANDA LLC	27dbf0bf-c273-2108-e063-6394a90a0a09	2025-11-10	Warnings	Exact identifier unii: 451W47IQ8X
Motofen	DIFENOXIN AND ATROPINE SULFATE	Sebela Pharmaceuticals Inc.	4cd3f029-a5e3-5812-e054-00144ff8d46c	2025-11-08	Warnings, Adverse reactions	Exact identifier unii: 03J5ZE7KA5
AZO Yeast Plus	CANDIDA ALBICANS, WOOD CREOSOTE, SODIUM CHLORIDE, AND SULFUR	i-Health, Inc.	22845cac-8011-4ea8-b35e-b72973eddb44	2025-11-07	Warnings	Exact identifier unii: 451W47IQ8X
SODIUM CHLORIDE	SODIUM CHLORIDE	Henry Schein, Inc.	2e81ffca-05c6-4fa0-8911-4b3cbfa71351	2025-11-07	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	Rising Pharma Holdings, Inc.	42870188-b1d7-4934-a6c0-310530497dac	2025-11-07	Warnings	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	Henry Schein, Inc.	d8b8d796-bfba-42af-a859-99d776871558	2025-11-07	Adverse reactions	Exact identifier unii: 451W47IQ8X
STERILE WATER	WATER	Henry Schein, Inc.	f4087143-9868-4308-b96c-43657ee8ec28	2025-11-07	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Bacteriostatic Sodium Chloride	SODIUM CHLORIDE	Henry Schein, Inc.	31188cdf-7bc8-4d78-bfaf-c1dc9f851fd4	2025-11-07	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Zilactin Early Relief Cold Sore	BENZYL ALCOHOL	ASCENT CONSUMER PRODUCTS, INC	42ef8bfa-c4d9-01cf-e063-6394a90ac88a	2025-11-06	Warnings	Exact identifier unii: LKG8494WBH
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE	B. Braun Medical Inc.	d3d29c8f-c326-4097-814a-7f4e08c67068	2025-11-05	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Ringers	SODIUM CHLORIDE, CALCIUM CHLORIDE, AND POTASSIUM CHLORIDE	B. Braun Medical Inc.	01721071-af03-4894-95c1-10b8bc64b888	2025-11-05	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Dextrose in Lactated Ringers	DEXTROSE, SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE	B. Braun Medical Inc.	190da07e-a616-46e6-b4e5-1c0ba39306e5	2025-11-05	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE	B. Braun Medical Inc.	f6d82772-638c-4584-b9d3-8833669f5963	2025-11-05	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Bacteriostatic Water	BACTERIOSTATIC WATER	ProPharma Distribution	42c6938e-f747-ae13-e063-6294a90a59a3	2025-11-04	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Com-Pare2 Dual Yeast Relief Plus Multi-symptom Formula	CANDIDA ALBICANS, WOOD CREOSOTE, SODIUM CHLORIDE, SULPHUR	TRP Company	42b6b9b9-a673-0bba-e063-6394a90a8866	2025-11-03	Warnings	Exact identifier unii: 451W47IQ8X
Potassium Chloride in Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, AND POTASSIUM CHLORIDE	ICU Medical Inc.	d8ee14e9-6733-4813-9f21-2b043a5f7188	2025-11-02	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE AND SODIUM CHLORIDE	ICU Medical Inc.	4555b1bf-6d97-4798-a63d-6d34291c85ce	2025-11-02	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sterile Water	WATER	ICU Medical Inc.	aab10f03-26ae-4dbc-a481-ef025e48b405	2025-11-02	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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