AQUASOL A - 61703-418-07 - (VITAMIN A PALMITATE)

Alphabetical Index


Drug Information of AQUASOL A

Product NDC: 61703-418
Proprietary Name: AQUASOL A
Non Proprietary Name: VITAMIN A PALMITATE
Active Ingredient(s): 15    mg/mL & nbsp;   VITAMIN A PALMITATE
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of AQUASOL A

Product NDC: 61703-418
Labeler Name: Hospira Worldwide, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA006823
Marketing Category: NDA
Start Marketing Date: 19490518

Package Information of AQUASOL A

Package NDC: 61703-418-07
Package Description: 10 VIAL, SINGLE-DOSE in 1 BOX (61703-418-07) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of AQUASOL A

NDC Code 61703-418-07
Proprietary Name AQUASOL A
Package Description 10 VIAL, SINGLE-DOSE in 1 BOX (61703-418-07) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 61703-418
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VITAMIN A PALMITATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 19490518
Marketing Category Name NDA
Labeler Name Hospira Worldwide, Inc.
Substance Name VITAMIN A PALMITATE
Strength Number 15
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of AQUASOL A


General Information