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Chlorthalidone
Chlorthalidone - 21695-671-30 - (chlorthalidone)
Drug Information of Chlorthalidone
| Product NDC: | 21695-671 |
| Proprietary Name: | Chlorthalidone |
| Non Proprietary Name: | chlorthalidone |
| Active Ingredient(s): | 25 mg/1 & nbsp; chlorthalidone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlorthalidone
| Product NDC: | 21695-671 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA086831 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091118 |
Package Information of Chlorthalidone
| Package NDC: | 21695-671-30 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (21695-671-30) |
NDC Information of Chlorthalidone
| NDC Code | 21695-671-30 |
| Proprietary Name | Chlorthalidone |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (21695-671-30) |
| Product NDC | 21695-671 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | chlorthalidone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091118 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CHLORTHALIDONE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide-like Diuretic [EPC] |
