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 |