NDC 0409-7447-16 - Cimetidine in Sodium Chloride

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: 0409-7447
Requested NDC: 0409-7447-16
Package NDCs from labels: 0409-7447-16
Manufacturer: HOSPIRA, INC.
Effective date: 2006-04-13
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
CIMETIDINE in 0.9% Sodium Chloride Injection, USP	HOSPIRA, INC.	2006-04-13	Human prescription drug label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Cimetidine	ACTIVE INGREDIENT	80061L1WGD	CIMETIDINE IN SODIUM CHLORIDE (CIMETIDINE AND SODIUM CHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Cimetidine	ACTIVE MOIETY	80061L1WGD	CIMETIDINE IN SODIUM CHLORIDE (CIMETIDINE AND SODIUM CHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Hydrochloric Acid	INACTIVE INGREDIENT	QTT17582CB	CIMETIDINE IN SODIUM CHLORIDE (CIMETIDINE AND SODIUM CHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Sodium Chloride	INACTIVE INGREDIENT	451W47IQ8X	CIMETIDINE IN SODIUM CHLORIDE (CIMETIDINE AND SODIUM CHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Sodium Hydroxide	INACTIVE INGREDIENT	55X04QC32I	CIMETIDINE IN SODIUM CHLORIDE (CIMETIDINE AND SODIUM CHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	CIMETIDINE IN SODIUM CHLORIDE (CIMETIDINE AND SODIUM CHLORIDE) 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 2 of 14 · 264 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Nalbuphine Hydrochloride	NALBUPHINE HYDROCHLORIDE	Hospira, Inc.	a99fe500-f52b-483c-807c-178f1a78a02b	2026-07-16	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium Chloride	SODIUM CHLORIDE	LABORATORIOS GRIFOLS SA	eb811d79-fdb8-1f1a-c2ad-1cc4bfc7eadf	2026-07-15	Warnings, Adverse reactions	Name fallback brand name: Sodium Chloride
Cimetidine	CIMETIDINE	Mylan Pharmaceuticals Inc.	06c0a509-026f-44e0-9975-a94a8de51d43	2026-07-15	Adverse reactions	Name fallback brand name: Cimetidine
Dextrose	DEXTROSE MONOHYDRATE	Hospira, Inc.	4ed365da-4e62-4329-c1b9-c197ab4fb6e1	2026-07-13	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Lorazepam	LORAZEPAM	Hospira, Inc.	20140b19-846b-425f-b191-670e17809945	2026-07-10	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Verapamil Hydrochloride	VERAPAMIL HYDROCHLORIDE	Hospira, Inc.	1c993365-1b62-4524-e781-d307f28f63bc	2026-07-09	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Procainamide Hydrochloride	PROCAINAMIDE HYDROCHLORIDE	Hospira, Inc.	17e47845-daad-434c-a784-6d3875b0d704	2026-07-08	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Paclitaxel	PACLITAXEL	Hospira, Inc.	ea28753a-8631-460a-bfdc-b101eb8ac84a	2026-07-02	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Nipent	PENTOSTATIN	Hospira, Inc.	674e0e6d-46ed-4868-9196-04019d667716	2026-07-01	Boxed warning, Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	Hospira, Inc.	559a0a8c-a8fe-40a5-b196-21f9308780ab	2026-07-01	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
CHROMIUM	CHROMIC CHLORIDE	Hospira, Inc.	b4d01ebb-a36e-44b7-028c-43c0ab2d13b4	2026-06-24	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Chromium	CHROMIC CHLORIDE	Hospira, Inc.	da207ca8-7836-4c66-92fe-36cc89baf773	2026-06-24	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Dextrose	DEXTROSE MONOHYDRATE	Hospira, Inc.	672264e3-9709-4bba-2a9d-12bf70c7396a	2026-06-24	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Marcaine Spinal	BUPIVACAINE HYDROCHLORIDE IN DEXTROSE	Hospira, Inc.	9679cc05-2f8a-4e88-53b5-6e9122c8b8c0	2026-06-23	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Linezolid	LINEZOLID	Hospira, Inc.	c401f1a8-cc37-461b-bfef-f2e156629bf8	2026-06-19	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Precedex	DEXMEDETOMIDINE HYDROCHLORIDE	Hospira, Inc.	92b7ddaa-e45a-4b64-a802-bb5df8771dd6	2026-06-17	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Sodium Chloride	SODIUM CHLORIDE	Cardinal Health 107, LLC	107af8bc-b6af-4b85-8c8a-ea757dcef1da	2026-06-12	Adverse reactions	Name fallback brand name: Sodium Chloride
Precedex	DEXMEDETOMIDINE HYDROCHLORIDE	Hospira, Inc.	4419162d-81d4-49bd-96de-1729440bdb74	2026-06-09	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Dobutamine in Dextrose	DOBUTAMINE IN DEXTROSE	Hospira, Inc.	9943a961-3b50-4847-8a84-d8414ce38daa	2026-06-03	Warnings, Adverse reactions	Name fallback manufacturer name: Hospira, Inc.
Dextrose	DEXTROSE MONOHYDRATE	Hospira, Inc.	10e98cb0-31a5-4ad1-3eaa-aa4af387a42d	2026-06-02	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.