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NDC 70710-1877-07 zinc sulfate 3 mg/mL Details
zinc sulfate 3 mg/mL
zinc sulfate is a INTRAVENOUS SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is ZINC SULFATE.
Product Information
| NDC | 70710-1877 |
|---|---|
| Product ID | 70710-1877_7bf7761a-873d-48bc-b884-818f16215689 |
| Associated GPIs | |
| GCN Sequence Number | 080056 |
| GCN Sequence Number Description | zinc sulfate VIAL 3 MG/ML INTRAVEN |
| HIC3 | C3C |
| HIC3 Description | ZINC REPLACEMENT |
| GCN | 46728 |
| HICL Sequence Number | 000744 |
| HICL Sequence Number Description | ZINC SULFATE |
| Brand/Generic | Generic |
| Proprietary Name | zinc sulfate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | zinc sulfate injection, |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 3 |
| Active Ingredient Units | mg/mL |
| Substance Name | ZINC SULFATE |
| Labeler Name | Zydus Pharmaceuticals USA Inc. |
| Pharmaceutical Class | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA217074 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70710-1877-07 (70710187707)
| NDC Package Code | 70710-1877-7 |
|---|---|
| Billing NDC | 70710187707 |
| Package | 25 VIAL in 1 CARTON (70710-1877-7) / 10 mL in 1 VIAL (70710-1877-1) |
| Marketing Start Date | 2023-12-07 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |