Midazolam

Product NDC

65293-414

11-digit product format

652930414

Labeler code

65293

Product ID

65293-414_99d569d6-86b7-560b-e053-2a95a90a0780

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

MIDAZOLAM HYDROCHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

The Medicines Company

Application

ANDA075154

Marketing category

ANDA

Marketing start

2000-07-14

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

2020-12-31

Current FDA listing

Historical FDA.report record