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DILT-CD
DILT-CD - 60505-0010-4 - (diltiazem hydrochloride)
Drug Information of DILT-CD
| Product NDC: | 60505-0010 |
| Proprietary Name: | DILT-CD |
| Non Proprietary Name: | diltiazem hydrochloride |
| Active Ingredient(s): | 300 mg/1 & nbsp; diltiazem hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DILT-CD
| Product NDC: | 60505-0010 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076151 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060830 |
Package Information of DILT-CD
| Package NDC: | 60505-0010-4 |
| Package Description: | 90 CAPSULE in 1 BOTTLE (60505-0010-4) |
NDC Information of DILT-CD
| NDC Code | 60505-0010-4 |
| Proprietary Name | DILT-CD |
| Package Description | 90 CAPSULE in 1 BOTTLE (60505-0010-4) |
| Product NDC | 60505-0010 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | diltiazem hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20060830 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
