MIDAZOLAM

Product NDC

51662-1236

11-digit product format

516621236

Labeler code

51662

Product ID

51662-1236_a09c4aaf-9109-211e-e053-2995a90ad8c2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

MIDAZOLAM

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

HF Acquisition Co LLC, DBA HealthFirst

Application

ANDA075856

Marketing category

ANDA

Marketing start

2018-09-16

Marketing end

2020-12-01

Substance

MIDAZOLAM HYDROCHLORIDE

Active strength

1 mg/mL

Pharmacologic classes

Benzodiazepine [EPC],Benzodiazepines [CS]

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record