NDC 0069-1311

RETACRIT

Epoetin Alfa-epbx

RETACRIT is a Intravenous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is Epoetin.

Product ID0069-1311_1b2796dd-509d-4a99-b464-48b8f3d2a217
NDC0069-1311
Product TypeHuman Prescription Drug
Proprietary NameRETACRIT
Generic NameEpoetin Alfa-epbx
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS; SUBCUTANEOUS
Marketing Start Date2020-11-09
Marketing CategoryBLA / BLA
Application NumberBLA125545
Labeler NamePfizer Laboratories Div Pfizer Inc
Substance NameEPOETIN
Active Ingredient Strength20000 [iU]/mL
Pharm ClassesErythropoiesis-stimulating Agent [EPC], Erythropoietin [CS], Increased Erythroid Cell Production [PE]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0069-1311-10

10 VIAL, MULTI-DOSE in 1 CARTON (0069-1311-10) > 1 mL in 1 VIAL, MULTI-DOSE (0069-1311-01)
Marketing Start Date2020-11-09
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "RETACRIT" or generic name "Epoetin Alfa-epbx"

NDCBrand NameGeneric Name
0069-1305RETACRITepoetin alfa-epbx
0069-1306RETACRITepoetin alfa-epbx
0069-1307RETACRITepoetin alfa-epbx
0069-1308RETACRITepoetin alfa-epbx
0069-1309RETACRITepoetin alfa-epbx
0069-1311RETACRITepoetin alfa-epbx
0069-1318RETACRITepoetin alfa-epbx
59353-004RETACRITRETACRIT
59353-002RETACRITRETACRIT
59353-003RETACRITRETACRIT
59353-010RETACRITRETACRIT
59353-120RETACRITRETACRIT
59353-220RETACRITRETACRIT

Trademark Results [RETACRIT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RETACRIT
RETACRIT
87340145 5770173 Live/Registered
Hospira, Inc.
2017-02-17
RETACRIT
RETACRIT
85028565 3925022 Dead/Cancelled
Hospira, Inc.
2010-05-03
RETACRIT
RETACRIT
77117569 not registered Dead/Abandoned
Hospira, Inc.
2007-02-27

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