NDC 0074-1824 - Novocain

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: 0074-1824
Package NDCs from labels: 0074-1824-30
Manufacturer: Hospira, Inc.
Effective date: 2007-04-16
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
NOVOCAIN ® PROCAINE HYDROCHLORIDE INJECTION, USP	Hospira, Inc.	2007-04-16	Human prescription drug label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0074-1824-30	Novocain	1 in 1 CARTON	INJECTION, SOLUTION	1		1
0074-1824-30	Novocain	100 in 1 CASE	INJECTION, SOLUTION	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0074-1824	NOVOCAIN (PROCAINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1	2 package rows	20070426_C80C810A-60E0-49BD-139C-95AEC3A286FC.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Procaine Hydrochloride	ACTIVE INGREDIENT	95URV01IDQ	NOVOCAIN (PROCAINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Procaine	ACTIVE MOIETY	4Z8Y51M438	NOVOCAIN (PROCAINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Acetone Sodium Bisulfite	INACTIVE INGREDIENT		NOVOCAIN (PROCAINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Chlorobutanol	INACTIVE INGREDIENT	HM4YQM8WRC	NOVOCAIN (PROCAINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Hydrochloric Acid	INACTIVE INGREDIENT	QTT17582CB	NOVOCAIN (PROCAINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Sodium Chloride	INACTIVE INGREDIENT	451W47IQ8X	NOVOCAIN (PROCAINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Sodium Hydroxide	INACTIVE INGREDIENT	55X04QC32I	NOVOCAIN (PROCAINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	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 11 of 13 · 253 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sodium Chloride	SODIUM CHLORIDE	CODAN US CORPORATION	aa06e286-75c6-4d7a-959f-6008d38aa6e5	2024-06-24	Warnings, Adverse reactions	Name fallback brand name: Sodium Chloride
Carboplatin	CARBOPLATIN	Hospira, Inc.	c3ae9880-44bb-4f4e-93d8-8a5e21708a30	2024-06-20	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
LEVETIRACETAM	LEVETIRACETAM	Hospira, Inc.	f1935bc8-30ce-4b51-8a4c-0f12ce9000a6	2024-06-05	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Aztreonam	AZTREONAM	Hospira, Inc.	d4500795-3b07-4a7d-b432-73cafbb3dbc6	2024-06-03	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium chloride	SODIUM CHLORIDE	Fresenius Kabi USA, LLC	239a5af1-7498-480f-862c-ab7c3d89d183	2024-05-21	Warnings, Adverse reactions	Name fallback brand name: Sodium chloride
Sodium chloride	SODIUM CHLORIDE	Becton Dickinson and Company	ebc8b008-a8b3-4c41-89e4-b413f7aab89f	2024-05-21	Warnings, Adverse reactions	Name fallback brand name: Sodium chloride
LEVETIRACETAM	LEVETIRACETAM	Hospira, Inc.	ed1b74a8-2a9b-4315-b051-673c7941cb13	2024-05-14	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium Chloride	SODIUM CHLORIDE	B. Braun Medical Inc.	47a0313f-36df-4fa6-a828-c9e1946ba9b0	2024-05-08	Warnings, Adverse reactions	Name fallback brand name: Sodium Chloride
Sodium Chloride	SODIUM CHLORIDE	B. Braun Medical Inc.	7f22c06b-6b4d-4b49-a4b2-d2169f2bd653	2024-05-07	Warnings, Adverse reactions	Name fallback brand name: Sodium Chloride
Sodium Chloride	SODIUM CHLORIDE	B. Braun Medical Inc.	f2475fa3-ab1d-4b81-8127-b58cd0790a54	2024-05-06	Warnings, Adverse reactions	Name fallback brand name: Sodium Chloride
Sodium chloride	SODIUM CHLORIDE	Fresenius Kabi USA, LLC	c1e52670-c85e-4f19-a2e9-bf9abd7c3727	2024-04-23	Warnings, Adverse reactions	Name fallback brand name: Sodium chloride
carboprost tromethamine	CARBOPROST TROMETHAMINE	Hospira, Inc.	e5054c6a-c54e-4ddf-8280-a154b90cac07	2024-04-15	Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium Chloride	SODIUM CHLORIDE	Hikma Pharmaceuticals USA Inc.	e5ee8caa-b6ca-45ba-98fb-8305e6282141	2024-04-10	Adverse reactions	Name fallback brand name: Sodium Chloride
Bortezomib	BORTEZOMIB	Hospira, Inc.	41e3de39-8278-4a75-badf-601e4602080d	2024-04-09	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Marcaine with Epinephrine	BUPIVACAINE HYDROCHLORIDE AND EPINEPHRINE	Hospira, Inc.	93cf0914-de08-4ec6-8f8c-d663243b9958	2024-02-02	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium Chloride	SODIUM CHLORIDE	Spectra Medical Deviecs, LLC	7e316d21-d6ad-4976-bd90-268fd7e51361	2024-01-12	Adverse reactions	Name fallback brand name: Sodium Chloride
Diazepam	DIAZEPAM	Hospira, Inc.	41044928-dd1f-40bf-1fa6-709dff559124	2024-01-05	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium chloride	SODIUM CHLORIDE	Fresenius Kabi USA, LLC	037ac04d-f8f3-4bb8-993a-ac8f7683ff83	2024-01-04	Warnings, Adverse reactions	Name fallback brand name: Sodium chloride
Atracurium Besylate	ATRACURIUM BESYLATE	Hospira, Inc.	de1c2dcd-295b-47ce-b7a1-a8be59939a54	2023-11-23	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
rocuronium bromide	ROCURONIUM BROMIDE	Hospira, Inc.	f01f9986-43f9-40e8-9506-11bfe78f9242	2023-08-29	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.

Reported adverse events (FAERS/openFDA)#

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