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Diltiazem Hydrochloride
Diltiazem Hydrochloride - 49884-832-11 - (Diltiazem Hydrochloride)
Drug Information of Diltiazem Hydrochloride
| Product NDC: | 49884-832 |
| Proprietary Name: | Diltiazem Hydrochloride |
| Non Proprietary Name: | Diltiazem Hydrochloride |
| Active Ingredient(s): | 300 mg/1 & nbsp; Diltiazem Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diltiazem Hydrochloride
| Product NDC: | 49884-832 |
| Labeler Name: | Par Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074984 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19991224 |
Package Information of Diltiazem Hydrochloride
| Package NDC: | 49884-832-11 |
| Package Description: | 30 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (49884-832-11) |
NDC Information of Diltiazem Hydrochloride
| NDC Code | 49884-832-11 |
| Proprietary Name | Diltiazem Hydrochloride |
| Package Description | 30 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (49884-832-11) |
| Product NDC | 49884-832 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diltiazem Hydrochloride |
| Dosage Form Name | CAPSULE, COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19991224 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical, Inc. |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
