Pentobarbital Sodium

Product NDC

70655-501

11-digit product format

706550501

Labeler code

70655

Product ID

70655-501_2797ced2-5af3-4497-bf28-a0e923118644

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

pentobarbital sodium

Dosage form

INJECTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Renaissance SSA, LLC

Application

ANDA206677

Marketing category

ANDA

Marketing start

2019-12-28

Marketing end

0000-00-00

Substance

PENTOBARBITAL SODIUM

Active strength

50 mg/mL

DEA schedule

CII

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record