zinc chloride

Generic: zinc chloride

Labeler: somerset therapeutics, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zinc chloride
Generic Name zinc chloride
Labeler somerset therapeutics, llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

zinc chloride 1 mg/mL

Manufacturer
Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-526
Product ID 70069-526_6b701c2f-faba-4d1a-ad8d-bebaf0ec7cfa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216152
Listing Expiration 2026-12-31
Marketing Start 2024-10-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70069526
Hyphenated Format 70069-526

Supplemental Identifiers

RxCUI
237508
UPC
0370069526019
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 ANDA216152 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 25 VIAL, PLASTIC in 1 CARTON (70069-526-25) / 10 mL in 1 VIAL, PLASTIC (70069-526-01)
source: ndc

Packages (1)

70069-526-25 25 VIAL, PLASTIC in 1 CARTON (70069-526-25) / 10 mL in 1 VIAL, PLASTIC (70069-526-01)

Ingredients (1)

zinc chloride (1 mg/mL)

Linked Drug Pages (1)

Zinc Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "6b701c2f-faba-4d1a-ad8d-bebaf0ec7cfa", "openfda": {"upc": ["0370069526019"], "unii": ["86Q357L16B"], "rxcui": ["237508"], "spl_set_id": ["9a4f7a7b-26d0-4292-bc7b-6ca9fa48600f"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, PLASTIC in 1 CARTON (70069-526-25)  / 10 mL in 1 VIAL, PLASTIC (70069-526-01)", "package_ndc": "70069-526-25", "marketing_start_date": "20241016"}], "brand_name": "Zinc Chloride", "product_id": "70069-526_6b701c2f-faba-4d1a-ad8d-bebaf0ec7cfa", "dosage_form": "INJECTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "70069-526", "generic_name": "Zinc Chloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zinc Chloride", "active_ingredients": [{"name": "ZINC CHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA216152", "marketing_category": "ANDA", "marketing_start_date": "20241016", "listing_expiration_date": "20261231"}