Home
>
National Drug Code (NDC)
>
THALITONE
THALITONE - 61570-024-01 - (chlorthalidone)
Drug Information of THALITONE
| Product NDC: | 61570-024 |
| Proprietary Name: | THALITONE |
| Non Proprietary Name: | chlorthalidone |
| Active Ingredient(s): | 15 mg/1 & nbsp; chlorthalidone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of THALITONE
| Product NDC: | 61570-024 |
| Labeler Name: | Monarch Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019574 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19881220 |
Package Information of THALITONE
| Package NDC: | 61570-024-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (61570-024-01) |
NDC Information of THALITONE
| NDC Code | 61570-024-01 |
| Proprietary Name | THALITONE |
| Package Description | 100 TABLET in 1 BOTTLE (61570-024-01) |
| Product NDC | 61570-024 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | chlorthalidone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19881220 |
| Marketing Category Name | NDA |
| Labeler Name | Monarch Pharmaceuticals, Inc |
| Substance Name | CHLORTHALIDONE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide-like Diuretic [EPC] |
