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Nembutal Sodium
Nembutal Sodium - 76478-501-20 - (pentobarbital sodium)
Drug Information of Nembutal Sodium
| Product NDC: | 76478-501 |
| Proprietary Name: | Nembutal Sodium |
| Non Proprietary Name: | pentobarbital sodium |
| Active Ingredient(s): | 50 mg/mL & nbsp; pentobarbital sodium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nembutal Sodium
| Product NDC: | 76478-501 |
| Labeler Name: | Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083246 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19730919 |
Package Information of Nembutal Sodium
| Package NDC: | 76478-501-20 |
| Package Description: | 1 VIAL in 1 CARTON (76478-501-20) > 20 mL in 1 VIAL |
NDC Information of Nembutal Sodium
| NDC Code | 76478-501-20 |
| Proprietary Name | Nembutal Sodium |
| Package Description | 1 VIAL in 1 CARTON (76478-501-20) > 20 mL in 1 VIAL |
| Product NDC | 76478-501 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | pentobarbital sodium |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19730919 |
| Marketing Category Name | ANDA |
| Labeler Name | Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.) |
| Substance Name | PENTOBARBITAL SODIUM |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
