Panhematin

Product NDC

55292-701

11-digit product format

552920701

Labeler code

55292

Product ID

55292-701_cdfd9947-bc51-43c9-9bd0-130c214bb68a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

hemin

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS

Labeler

RECORDATI RARE DISEASES, INC.

Application

BLA101246

Marketing category

BLA

Marketing start

1983-07-20

Marketing end

2020-01-24

Substance

HEMIN

Active strength

7 mg/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record