NDC 0010-4712 - POLYFLEX

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: 0010-4712
Package NDCs from labels: 0010-4712-02
Manufacturer: Boehringer Ingelheim Animal Health USA Inc.
Effective date: 2024-09-17
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Polyflex® (ampicillin for injectable suspension)	Boehringer Ingelheim Animal Health USA Inc.	2024-09-17	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0010-4712-02	POLYFLEX	79 mL in 1 VIAL	INJECTION, POWDER, FOR SUSPENSIO	79		10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0010-4712	POLYFLEX (AMPICILLIN) INJECTION, POWDER, FOR SUSPENSION [BOEHRINGER INGELHEIM ANIMAL HEALTH USA INC.]	10	1 package rows	20240919_61be8261-ac3d-418a-a414-62c64d9eacc0.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
AMPICILLIN TRIHYDRATE	ACTIVE INGREDIENT	HXQ6A1N7R6	POLYFLEX (AMPICILLIN FOR INJECTABLE SUSPENSION) INJECTION, POWDER, FOR SUSPENSION [BOEHRINGER INGELHEIM VETMEDICA, INC.]	3
AMPICILLIN	ACTIVE MOIETY	7C782967RD	POLYFLEX (AMPICILLIN FOR INJECTABLE SUSPENSION) INJECTION, POWDER, FOR SUSPENSION [BOEHRINGER INGELHEIM VETMEDICA, INC.]	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 45 of 45 · 881 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12		Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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