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NDC 68083-0608-25 Zinc Sulfate 1 mg/mL Details
Zinc Sulfate 1 mg/mL
Zinc Sulfate is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Gland Pharma Limited. The primary component is ZINC SULFATE.
Product Information
| NDC | 68083-0608 |
|---|---|
| Product ID | 68083-608_cfa59996-1de2-4313-a7ac-1766764513e2 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Zinc Sulfate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Zinc Sulfate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 1 |
| Active Ingredient Units | mg/mL |
| Substance Name | ZINC SULFATE |
| Labeler Name | Gland Pharma Limited |
| Pharmaceutical Class | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA216249 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68083-0608-25 (68083060825)
| NDC Package Code | 68083-608-25 |
|---|---|
| Billing NDC | 68083060825 |
| Package | 25 VIAL in 1 CARTON (68083-608-25) / 10 mL in 1 VIAL |
| Marketing Start Date | 2023-09-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |