AQUASOL A
AQUASOL A Parenteral
Approved
Approval ID
ec825f1c-c15f-44de-ad46-8ab9c49ec21c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 14, 2020
Manufacturers
FDA
Casper Pharma LLC
DUNS: 080025838
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
VITAMIN A PALMITATE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70199-026
Application NumberNDA006823
Product Classification
M
Marketing Category
C73594
G
Generic Name
VITAMIN A PALMITATE
Product Specifications
Route of AdministrationINTRAMUSCULAR
Effective DateAugust 14, 2020
FDA Product Classification
INGREDIENTS (5)
VITAMIN A PALMITATEActive
Quantity: 15 mg in 1 mL
Code: 1D1K0N0VVC
Classification: ACTIM
CHLOROBUTANOLInactive
Code: HM4YQM8WRC
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
CITRIC ACID MONOHYDRATEInactive
Code: 2968PHW8QP
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT