NDC 70655-501
Pentobarbital Sodium
Pentobarbital Sodium
Pentobarbital Sodium is a Intramuscular; Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Renaissance Ssa, Llc. The primary component is Pentobarbital Sodium.
Product ID | 70655-501_2797ced2-5af3-4497-bf28-a0e923118644 |
NDC | 70655-501 |
Product Type | Human Prescription Drug |
Proprietary Name | Pentobarbital Sodium |
Generic Name | Pentobarbital Sodium |
Dosage Form | Injection |
Route of Administration | INTRAMUSCULAR; INTRAVENOUS |
Marketing Start Date | 2019-12-28 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA206677 |
Labeler Name | Renaissance SSA, LLC |
Substance Name | PENTOBARBITAL SODIUM |
Active Ingredient Strength | 50 mg/mL |
DEA Schedule | CII |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |