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FDA Approval

Eliphos

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
Effective Date
August 6, 2016
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Calcium acetate(667 mg in 1 1)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Carilion Materials Management

Carilion Materials Management

079239644

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Eliphos

Product Details

NDC Product Code
68151-5204
Application Number
ANDA078502
Marketing Category
ANDA (C73584)
Route of Administration
ORAL
Effective Date
September 3, 2015
Code: Y882YXF34XClass: ACTIBQuantity: 667 mg in 1 1
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