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Diltiazem Hydrochloride
Diltiazem Hydrochloride - 63739-284-10 - (Diltiazem Hydrochloride)
Drug Information of Diltiazem Hydrochloride
| Product NDC: | 63739-284 |
| Proprietary Name: | Diltiazem Hydrochloride |
| Non Proprietary Name: | Diltiazem Hydrochloride |
| Active Ingredient(s): | 180 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: | 63739-284 |
| Labeler Name: | McKesson Packaging Services Business Unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074984 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070621 |
Package Information of Diltiazem Hydrochloride
| Package NDC: | 63739-284-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-284-10) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Diltiazem Hydrochloride
| NDC Code | 63739-284-10 |
| Proprietary Name | Diltiazem Hydrochloride |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-284-10) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 63739-284 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diltiazem Hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20070621 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Services Business Unit of McKesson Corporation |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
