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Seconal Sodium
Seconal Sodium - 42998-679-01 - (secobarbital sodium)
Drug Information of Seconal Sodium
| Product NDC: | 42998-679 |
| Proprietary Name: | Seconal Sodium |
| Non Proprietary Name: | secobarbital sodium |
| Active Ingredient(s): | 100 mg/1 & nbsp; secobarbital sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Seconal Sodium
| Product NDC: | 42998-679 |
| Labeler Name: | Marathon Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA086101 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19831003 |
Package Information of Seconal Sodium
| Package NDC: | 42998-679-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (42998-679-01) |
NDC Information of Seconal Sodium
| NDC Code | 42998-679-01 |
| Proprietary Name | Seconal Sodium |
| Package Description | 100 CAPSULE in 1 BOTTLE (42998-679-01) |
| Product NDC | 42998-679 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | secobarbital sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19831003 |
| Marketing Category Name | ANDA |
| Labeler Name | Marathon Pharmaceuticals, LLC |
| Substance Name | SECOBARBITAL SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
