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Diltiazem HCl CD
Diltiazem HCl CD - 68682-521-01 - (Diltiazem Hydrochloride)
Drug Information of Diltiazem HCl CD
| Product NDC: | 68682-521 |
| Proprietary Name: | Diltiazem HCl CD |
| Non Proprietary Name: | Diltiazem Hydrochloride |
| Active Ingredient(s): | 360 mg/1 & nbsp; Diltiazem Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diltiazem HCl CD
| Product NDC: | 68682-521 |
| Labeler Name: | Oceanside Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020062 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20120718 |
Package Information of Diltiazem HCl CD
| Package NDC: | 68682-521-01 |
| Package Description: | 90 CAPSULE in 1 BOTTLE, PLASTIC (68682-521-01) |
NDC Information of Diltiazem HCl CD
| NDC Code | 68682-521-01 |
| Proprietary Name | Diltiazem HCl CD |
| Package Description | 90 CAPSULE in 1 BOTTLE, PLASTIC (68682-521-01) |
| Product NDC | 68682-521 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diltiazem Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120718 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Oceanside Pharmaceuticals |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 360 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
