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NDC 71335-1223-02 Diltiazem Hydrochloride 120 mg/1 Details
Diltiazem Hydrochloride 120 mg/1
Diltiazem Hydrochloride is a ORAL CAPSULE, COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is DILTIAZEM HYDROCHLORIDE.
Product Information
| NDC | 71335-1223 |
|---|---|
| Product ID | 71335-1223_25662185-7ac5-489e-82fd-378a6cb2d974 |
| Associated GPIs | 34000010127020 |
| GCN Sequence Number | 021282 |
| GCN Sequence Number Description | diltiazem HCl CAP ER 24H 120 MG ORAL |
| HIC3 | A9A |
| HIC3 Description | CALCIUM CHANNEL BLOCKING AGENTS |
| GCN | 02326 |
| HICL Sequence Number | 000182 |
| HICL Sequence Number Description | DILTIAZEM HCL |
| Brand/Generic | Generic |
| Proprietary Name | Diltiazem Hydrochloride |
| Proprietary Name Suffix | Extended-Release |
| Non-Proprietary Name | Diltiazem Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CAPSULE, COATED, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 120 |
| Active Ingredient Units | mg/1 |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Labeler Name | Bryant Ranch Prepack |
| Pharmaceutical Class | Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA074984 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 71335-1223-02 (71335122302)
| NDC Package Code | 71335-1223-2 |
|---|---|
| Billing NDC | 71335122302 |
| Package | 90 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1223-2) |
| Marketing Start Date | 2021-05-19 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |