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Biltricide
Biltricide - 0085-1747-01 - (praziquantel)
Drug Information of Biltricide
| Product NDC: | 0085-1747 |
| Proprietary Name: | Biltricide |
| Non Proprietary Name: | praziquantel |
| Active Ingredient(s): | 600 mg/1 & nbsp; praziquantel |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Biltricide
| Product NDC: | 0085-1747 |
| Labeler Name: | Schering Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018714 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100816 |
Package Information of Biltricide
| Package NDC: | 0085-1747-01 |
| Package Description: | 6 TABLET, FILM COATED in 1 BOTTLE (0085-1747-01) |
NDC Information of Biltricide
| NDC Code | 0085-1747-01 |
| Proprietary Name | Biltricide |
| Package Description | 6 TABLET, FILM COATED in 1 BOTTLE (0085-1747-01) |
| Product NDC | 0085-1747 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | praziquantel |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100816 |
| Marketing Category Name | NDA |
| Labeler Name | Schering Corporation |
| Substance Name | PRAZIQUANTEL |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antihelminthic [EPC] |
