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Doxycycline Hyclate

NDC 69668-515 · Sonoma Pharmaceuticals, Inc.

Generic nameDOXYCYCLINE HYCLATE
Dosage formTABLET, DELAYED RELEASE
RouteORAL
Active ingredient(s)DOXYCYCLINE HYCLATE
Strength150 mg/1
Pharmacologic classTetracycline-class Drug [EPC], Tetracyclines [CS]
Marketing categoryANDA

Packages

69668-515-30 — 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69668-515-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-4176 — doxycycline, 68788-8588 — doxycycline, 68999-625 — Doxycycline Hyclate, 68999-626 — Doxycycline Hyclate, 68999-984 — doxycycline hyclate, 68999-985 — doxycycline hyclate, 69238-1100 — Doxycycline, 69434-016 — Doxycycline Hyclate, 69434-017 — Doxycycline Hyclate, 69489-111 — doxycycline hyclate, 70121-1616 — Doxycycline, 70518-1248 — Doxycycline Hyclate, 70518-1627 — Doxycycline Hyclate, 70518-3039 — Doxycycline hyclate, 70518-3213 — Doxycycline Hyclate, 70518-3214 — Doxycycline Hyclate, 70518-3363 — Doxycycline hyclate, 70518-3488 — doxycycline, 70518-3869 — DOXYCYCLINE HYCLATE, 70518-4150 — Doxycycline hyclate, +199 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.