zinc chloride
Generic: zinc chloride
Labeler: exela pharma sciences,llcDrug Facts
Product Profile
Brand Name
zinc chloride
Generic Name
zinc chloride
Labeler
exela pharma sciences,llc
Dosage Form
INJECTION
Routes
Active Ingredients
zinc chloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51754-0102
Product ID
51754-0102_5f09a6b3-abb1-4d80-9ed9-88a343ea472b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212007
Listing Expiration
2026-12-31
Marketing Start
2021-08-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
517540102
Hyphenated Format
51754-0102
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
zinc chloride (source: ndc)
Generic Name
zinc chloride (source: ndc)
Application Number
ANDA212007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 25 VIAL in 1 CARTON (51754-0102-4) / 10 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "5f09a6b3-abb1-4d80-9ed9-88a343ea472b", "openfda": {"unii": ["86Q357L16B"], "rxcui": ["237508"], "spl_set_id": ["2bd646d2-2a2a-4376-8da0-c7f08b0511ac"], "manufacturer_name": ["Exela Pharma Sciences,LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (51754-0102-4) / 10 mL in 1 VIAL", "package_ndc": "51754-0102-4", "marketing_start_date": "20210827"}], "brand_name": "Zinc Chloride", "product_id": "51754-0102_5f09a6b3-abb1-4d80-9ed9-88a343ea472b", "dosage_form": "INJECTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "51754-0102", "generic_name": "Zinc Chloride", "labeler_name": "Exela Pharma Sciences,LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zinc Chloride", "active_ingredients": [{"name": "ZINC CHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA212007", "marketing_category": "ANDA", "marketing_start_date": "20210827", "listing_expiration_date": "20261231"}