ATROPINE SULFATE

Product NDC

50090-2181

11-digit product format

500902181

Labeler code

50090

Product ID

50090-2181_0ef7e127-3f97-4252-b8d1-437c72551553

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ATROPINE SULFATE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

A-S Medication Solutions

Application

NDA021146

Marketing category

NDA

Marketing start

2005-10-25

Marketing end

0000-00-00

Substance

ATROPINE SULFATE

Active strength

0 mg/mL

Pharmacologic classes

Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record