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diltiazem hydrochloride
diltiazem hydrochloride - 0258-3692-90 - (diltiazem hydrochloride)
Drug Information of diltiazem hydrochloride
| Product NDC: | 0258-3692 |
| Proprietary Name: | diltiazem hydrochloride |
| Non Proprietary Name: | diltiazem hydrochloride |
| Active Ingredient(s): | 420 mg/1 & nbsp; diltiazem hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of diltiazem hydrochloride
| Product NDC: | 0258-3692 |
| Labeler Name: | Forest Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020401 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20090925 |
Package Information of diltiazem hydrochloride
| Package NDC: | 0258-3692-90 |
| Package Description: | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0258-3692-90) |
NDC Information of diltiazem hydrochloride
| NDC Code | 0258-3692-90 |
| Proprietary Name | diltiazem hydrochloride |
| Package Description | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0258-3692-90) |
| Product NDC | 0258-3692 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | diltiazem hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090925 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Forest Laboratories, Inc. |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 420 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
