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 9 of 13 · 253 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Testosterone Cypionate	TESTOSTERONE CYPIONATE	Hospira, Inc.	6909596e-4bf7-4e11-8029-b89740a30aec	2025-08-22	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium Chloride	SODIUM CHLORIDE	Henry Schein, Inc.	e0466bb3-6c26-4044-b051-69f48b67f632	2025-08-07	Adverse reactions	Name fallback brand name: Sodium Chloride
SODIUM CHLORIDE	SODIUM CHLORIDE	Baxter Healthcare Corporation	9e72418a-376e-4637-99ad-d13c904a7986	2025-07-30	Warnings, Adverse reactions	Name fallback brand name: SODIUM CHLORIDE
Sodium Chloride	SODIUM CHLORIDE	Nextgen Pharmaceuticals LLC	28f79c75-82d2-4912-81fc-a723b5ccf4c1	2025-07-23	Warnings, Adverse reactions	Name fallback brand name: Sodium Chloride
Mitoxantrone	MITOXANTRONE	Hospira, Inc.	accf9569-4b57-4e83-a7db-4e890a75d1ba	2025-07-14	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium Chloride	SODIUM CHLORIDE	B. Braun Medical Inc.	0d59a04a-32e6-485b-b638-a1e6c09e9642	2025-07-09	Warnings, Adverse reactions	Name fallback brand name: Sodium Chloride
Methotrexate	METHOTREXATE	Hospira, Inc.	bd287e89-32f9-4396-95fa-4b562869f476	2025-06-30	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
SODIUM CHLORIDE	SODIUM CHLORIDE	Baxter Healthcare Corporation	958d35f0-6834-43be-a700-fa58f38b4c19	2025-06-30	Warnings, Adverse reactions	Name fallback brand name: SODIUM CHLORIDE
LEVOPHED	NOREPINEPHRINE BITARTRATE	Hospira, Inc.	2c7dd2b0-cc10-4db6-bf56-6eb154ebeb10	2025-06-12	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
LEVOPHED	NOREPINEPHRINE BITARTRATE	Hospira, Inc.	c4de72a8-2a75-4984-ce90-e4870226dc12	2025-06-12	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Methotrexate	METHOTREXATE	Hospira, Inc.	0d63ba29-b692-41b4-87e8-351265c8273f	2025-06-10	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium chloride	SODIUM CHLORIDE	Fresenius Kabi USA, LLC	6d43fa91-0940-437f-ba70-b2d3f977593e	2025-04-25	Warnings, Adverse reactions	Name fallback brand name: Sodium chloride
Cytarabine	CYTARABINE	Hospira, Inc.	e3a8c0e9-19ed-49b7-8464-11e8806f47fd	2025-04-07	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium Chloride	SODIUM CHLORIDE TABLET	Belleview Bioscience LLC	31195e8f-d4de-9e37-e063-6294a90a4156	2025-03-24	Warnings	Name fallback brand name: Sodium Chloride
Docetaxel	DOCETAXEL	Hospira, Inc.	6b9999bb-869e-4d25-838c-23c3ab280044	2025-01-31	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium Chloride	SODIUM CHLORIDE	Baxter Healthcare Corporation	93aeac13-41de-4452-9f38-d6b4f38ada30	2025-01-24		Name fallback brand name: Sodium Chloride
Docetaxel	DOCETAXEL ANHYDROUS	Hospira, Inc.	644c5035-20d2-4686-beaa-bef08e99051c	2025-01-20	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Docetaxel	DOCETAXEL ANHYDROUS	Hospira, Inc.	00c61d11-d6b7-4618-b6f6-2592dbcc8af7	2025-01-20	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Vancomycin Hydrochloride	VANCOMYCIN HYDROCHLORIDE	Hospira, Inc.	91c050cf-3b2d-48bc-7297-e8dc68225e5a	2025-01-16	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
SODIUM CHLORIDE	SODIUM CHLORIDE	HF Acquisition Co LLC, DBA HealthFirst	998a2a47-5c79-2efd-e053-2995a90a8fac	2025-01-08	Adverse reactions	Name fallback brand name: SODIUM CHLORIDE

Reported adverse events (FAERS/openFDA)#

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