Aurovisc OE
Approved
Approval ID
3142c6df-77ac-ec41-e063-6294a90aee47
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Mar 24, 2025
Manufacturers
FDA
Aurolab
DUNS: 677319965
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Hypromellose Ophthalmic Solution 2% w/v
PRODUCT DETAILS
NDC Product Code16030-304
Application NumberM018
Marketing CategoryC200263
Route of AdministrationOPHTHALMIC
Effective DateMarch 24, 2025
Generic NameHypromellose Ophthalmic Solution 2% w/v
INGREDIENTS (10)
SODIUM ACETATEInactive
Code: 4550K0SC9B
Classification: IACT
POTASSIUM CHLORIDEInactive
Code: 660YQ98I10
Classification: IACT
CITRIC ACID ACETATEInactive
Code: DSO12WL7AU
Classification: IACT
HYPROMELLOSE 2208 (15000 MPA.S)Active
Quantity: 20 mg in 1 mL
Code: Z78RG6M2N2
Classification: ACTIB
SODIUM CITRATEInactive
Code: 1Q73Q2JULR
Classification: IACT
CALCIUM CHLORIDEInactive
Code: M4I0D6VV5M
Classification: IACT
ACETIC ACIDInactive
Code: Q40Q9N063P
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
MAGNESIUM CHLORIDEInactive
Code: 02F3473H9O
Classification: IACT