Midazolam

Product NDC

50090-3312

11-digit product format

500903312

Labeler code

50090

Product ID

50090-3312_e2e50e9b-e69b-481a-a9e6-38049cab3374

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

midazolam hydrochloride

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

A-S Medication Solutions

Application

ANDA090850

Marketing category

ANDA

Marketing start

2016-12-14

Marketing end

0000-00-00

Substance

MIDAZOLAM HYDROCHLORIDE

Active strength

5 mg/mL

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record