doxycycline hyclate
Doxycycline Hyclate Capsules, USP Doxycycline for Oral Suspension, USP Doxycycline Hyclate Tablets, USP
Approved
Approval ID
4164f6b7-5ebd-4f5f-a536-9a37b2e0562c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 7, 2024
Manufacturers
FDA
A-S Medication Solutions
DUNS: 830016429
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
doxycycline hyclate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code50090-5588
Application NumberANDA062500
Product Classification
M
Marketing Category
C73584
G
Generic Name
doxycycline hyclate
Product Specifications
Route of AdministrationORAL
Effective DateOctober 10, 2023
FDA Product Classification
INGREDIENTS (1)
DOXYCYCLINE HYCLATEActive
Quantity: 100 mg in 1 1
Code: 19XTS3T51U
Classification: ACTIM