zinc chloride

Generic: zinc chloride

Labeler: exela pharma sciences,llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zinc chloride
Generic Name zinc chloride
Labeler exela pharma sciences,llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

zinc chloride 1 mg/mL

Manufacturer
Exela Pharma Sciences,LLC

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
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 517540102
Hyphenated Format 51754-0102

Supplemental Identifiers

RxCUI
237508
UNII
86Q357L16B

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (51754-0102-4) / 10 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

zinc chloride (1 mg/mL)

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"}