Adenosine

Product NDC

70518-1232

11-digit product format

705181232

Labeler code

70518

Product ID

70518-1232_a340ff9a-ee27-0522-e053-2a95a90aed80

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ADENOSINE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

REMEDYREPACK INC.

Application

ANDA077133

Marketing category

ANDA

Marketing start

2018-05-30

Marketing end

0000-00-00

Substance

ADENOSINE

Active strength

3 mg/mL

Pharmacologic classes

Adenosine Receptor Agonist [EPC],Adenosine Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record