Nembutal Sodium is a Intramuscular; Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Akron. The primary component is Pentobarbital Sodium.
Product ID | 76478-501_05af1063-ce0d-485f-a569-3345f6e1b761 |
NDC | 76478-501 |
Product Type | Human Prescription Drug |
Proprietary Name | Nembutal Sodium |
Generic Name | Pentobarbital Sodium |
Dosage Form | Injection |
Route of Administration | INTRAMUSCULAR; INTRAVENOUS |
Marketing Start Date | 1973-09-19 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA083246 |
Labeler Name | Akron |
Substance Name | PENTOBARBITAL SODIUM |
Active Ingredient Strength | 50 mg/mL |
DEA Schedule | CII |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 1973-09-19 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA083246 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1973-09-19 |
Marketing Category | ANDA |
Application Number | ANDA083246 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1973-09-19 |
Ingredient | Strength |
---|---|
PENTOBARBITAL SODIUM | 50 mg/mL |
SPL SET ID: | 5c380ab0-4386-48b6-80ab-ca594b23bc74 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
76478-501 | Nembutal Sodium | pentobarbital sodium |
17478-181 | Pentobarbital Sodium | Pentobarbital Sodium |
24201-010 | Pentobarbital Sodium | Pentobarbital Sodium |
25021-676 | pentobarbital sodium | pentobarbital sodium |
70655-501 | Pentobarbital Sodium | pentobarbital sodium |