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Doxycycline Hyclate

DOXYCYCLINE HYCLATE CAPSULES USP 50 mg and 100 mg DOXYCYCLINE HYCLATE TABLETS USP 100 mg

Approved
Approval ID

120b912d-87d4-4463-ae46-5e48ca33db49

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 8, 2012

Manufacturers
FDA

Life Line Home Care Services, Inc.

DUNS: 844985374

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 Code75921-119
Application NumberANDA062676
Product Classification
M
Marketing Category
C73584
G
Generic Name
Doxycycline Hyclate
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 8, 2012
FDA Product Classification

INGREDIENTS (9)

Doxycycline HyclateActive
Quantity: 100 mg in 1 1
Code: 19XTS3T51U
Classification: ACTIM
anhydrous lactoseInactive
Code: 3SY5LH9PMK
Classification: IACT
FD&C Blue No. 1Inactive
Code: H3R47K3TBD
Classification: IACT
gelatinInactive
Code: 2G86QN327L
Classification: IACT
magnesium stearateInactive
Code: 70097M6I30
Classification: IACT
cellulose, microcrystallineInactive
Code: OP1R32D61U
Classification: IACT
D&C Red No. 28Inactive
Code: 767IP0Y5NH
Classification: IACT
titanium dioxideInactive
Code: 15FIX9V2JP
Classification: IACT
croscarmellose sodiumInactive
Code: M28OL1HH48
Classification: IACT

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Doxycycline Hyclate - FDA Drug Approval Details