ZINC SULFATE 1 mg/mL
ZINC SULFATE · INJECTION, SOLUTION · Camber Pharmaceuticals, Inc.
ZINC SULFATE is a injection, solution containing zinc sulfate at 1 mg/mL, taken intravenous. Manufactured by Camber Pharmaceuticals, Inc..
Key Facts
- Brand Name
- ZINC SULFATE
- Generic Name
- ZINC SULFATE
- NDC Code (Product)
31722-453- Manufacturer
- Camber Pharmaceuticals, Inc.
- Strength
- 1 mg/mL
- Dosage Form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Marketing Status
- Application #
- ANDA219585
- Marketing Start
- 05/01/2025
Recall History
Lincare, Inc.
Lack of Assurance of Sterility: Sterility of product is not assured.
Promise Pharmacy, LLC
Lack of sterility assurance.
Aidapak Services, LLC
Labeling:Label Mixup; ZINC SULFATE Capsule, 220 mg may be potentially mislabeled as CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD52778_10, EXP: 5/20/2014; CALCITRIOL, Capsule, 0.25 mcg, NDC 00054000725, Pedigree: W003638, EXP: 6/25/2014.
Medtech Products, Inc.
CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Aidapak Services, LLC
Labeling: Label Mixup; ZINC SULFATE, Capsule, 50 mg may be potentially mislabeled as SERTRALINE HCL, Tablet, 50 mg, NDC 16714061204, Pedigree: AD30993_14, EXP: 5/9/2014.
Beacon Hill Medical Pharmacy, P.C.
Lack of Assurance of Sterility; FDA inspectional findings resulted in concerns associated with quality control procedures that impacted sterility assurance
First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy
Lack of Assurance of Sterility
Medtech Products, Inc.
CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Medtech Products, Inc.
CGMP Deviations: concerns regarding the sufficiency of Quality Assurance controls over critical systems in the manufacturing facility that could impact the product quality of the finished products.
Aidapak Services, LLC
Labeling: Label Mixup; ZINC SULFATE, Capsule, 220 mg (50 mg Elem Zn) may be potentially mislabeled as PHOSPHORUS, Tablet, 250 mg, NDC 64980010401, Pedigree: AD56916_1, EXP: 5/21/2014.
Side Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Frequently Asked Questions
What is ZINC SULFATE used for?
ZINC SULFATE contains ZINC SULFATE. It is a injection, solution taken intravenous. Consult your doctor for specific uses.
Is ZINC SULFATE a controlled substance?
ZINC SULFATE is not classified as a controlled substance by the DEA.
What is the generic name for ZINC SULFATE?
The generic name for ZINC SULFATE is ZINC SULFATE. There are 10 other brand versions of ZINC SULFATE.
What is the NDC code for ZINC SULFATE 1 mg/mL?
The NDC (National Drug Code) for ZINC SULFATE 1 mg/mL is 31722-453, listed by Camber Pharmaceuticals, Inc..
Other ZINC SULFATE Dosages
Other Zinc Brands
See all →- Zincum sulphuricum200 [kp_C]/200[kp_C]0220-5486
- Zinc Sulfate3 mg/mL65219-403
- Zinc Sulfate1 mg/mL66794-255
- zinc sulfate5 mg/mL70710-1878
- Zinc Sulfate1 mg/mL60505-6261
- Zinc Sulfate5 mg/mL65219-405
- zinc sulfate1 mg/mL70710-1876
- zinc sulfate5 mg/mL70771-1850
- zinc sulfate3 mg/mL70710-1877
- Zinc Sulfate3 mg/mL0517-6103
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)