NDC 0069-1306-01 - RETACRIT

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: 0069-1306
Requested NDC: 0069-1306-01
Package NDCs from labels: 0069-1306-01, 0069-1306-10
Manufacturer: Pfizer Laboratories Div Pfizer Inc | Hospira, Inc. | Eurofins PROXY Laboratories B.V.
Effective date: 2025-06-22
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
RETACRIT	Pfizer Laboratories Div Pfizer Inc \| Hospira, Inc. \| Eurofins PROXY Laboratories B.V.	2025-06-22	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0069-1306-01	RETACRIT	1 mL in 1 VIAL, SINGLE-DOSE	INJECTION, SOLUTION	1		19
0069-1306-10	RETACRIT	10 in 1 CARTON	INJECTION, SOLUTION	10		19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0069-1306	RETACRIT (EPOETIN ALFA-EPBX) INJECTION, SOLUTION [PFIZER LABORATORIES DIV PFIZER INC]	18	Current NDC, Legacy NDC, 2 package rows	20240621_3af26b0d-8ad0-44e1-a538-8bdb5ab39374.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0069-1306-01	ML - Milliliter	0069-1306	a6cf3542-2ad5-4594-998e-2a859d422ad6	1	2018-06-11
0069-1306-10	ML - Milliliter	0069-1306	e7909c6b-3133-4c33-b1be-1ae7300d84a4	1	2018-06-11

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 62 of 62 · 1,221 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 unii: M4I0D6VV5M

Reported adverse events (FAERS/openFDA)#

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