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Prazolamine
Prazolamine - 68405-028-06 - (CARISOPRODOL, GABA)
Drug Information of Prazolamine
| Product NDC: | 68405-028 |
| Proprietary Name: | Prazolamine |
| Non Proprietary Name: | CARISOPRODOL, GABA |
| Active Ingredient(s): | & nbsp; CARISOPRODOL, GABA |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prazolamine
| Product NDC: | 68405-028 |
| Labeler Name: | Physician Therapeutics LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110707 |
Package Information of Prazolamine
| Package NDC: | 68405-028-06 |
| Package Description: | 1 KIT in 1 KIT (68405-028-06) * 30 TABLET in 1 BOTTLE (52959-026-30) * 60 CAPSULE in 1 BOTTLE |
NDC Information of Prazolamine
| NDC Code | 68405-028-06 |
| Proprietary Name | Prazolamine |
| Package Description | 1 KIT in 1 KIT (68405-028-06) * 30 TABLET in 1 BOTTLE (52959-026-30) * 60 CAPSULE in 1 BOTTLE |
| Product NDC | 68405-028 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CARISOPRODOL, GABA |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110707 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Physician Therapeutics LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
