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Cartia - 62037-597-90 - (Diltiazem Hydrochloride)
Drug Information of Cartia
| Product NDC: | 62037-597 |
| Proprietary Name: | Cartia |
| Non Proprietary Name: | Diltiazem Hydrochloride |
| Active Ingredient(s): | 120 mg/1 & nbsp; Diltiazem Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cartia
| Product NDC: | 62037-597 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074752 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990623 |
Package Information of Cartia
| Package NDC: | 62037-597-90 |
| Package Description: | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-597-90) |
NDC Information of Cartia
| NDC Code | 62037-597-90 |
| Proprietary Name | Cartia |
| Package Description | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-597-90) |
| Product NDC | 62037-597 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diltiazem Hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19990623 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
