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Doxycycline Hyclate

NDC 46708-484 · Alembic Pharmaceuticals Limited

Generic nameDoxycycline Hyclate
Dosage formTABLET, DELAYED RELEASE
RouteORAL
Active ingredient(s)DOXYCYCLINE HYCLATE
Strength200 mg/1
Pharmacologic classTetracycline-class Drug [EPC], Tetracyclines [CS]
Marketing categoryANDA

Packages

46708-484-30 — 30 TABLET, DELAYED RELEASE in 1 BOTTLE (46708-484-30)

46708-484-31 — 100 TABLET, DELAYED RELEASE in 1 BOTTLE (46708-484-31)

46708-484-60 — 60 TABLET, DELAYED RELEASE in 1 BOTTLE (46708-484-60)

46708-484-71 — 500 TABLET, DELAYED RELEASE in 1 BOTTLE (46708-484-71)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43598-086 — DOXYCYCLINE, 46708-352 — Doxycycline Hyclate, 46708-353 — Doxycycline Hyclate, 46708-362 — doxycycline hyclate, 46708-363 — doxycycline hyclate, 46708-387 — DOXYCYCLINE HYCLATE, 46708-388 — DOXYCYCLINE HYCLATE, 46708-481 — Doxycycline Hyclate, 46708-482 — Doxycycline Hyclate, 46708-483 — Doxycycline Hyclate, 46708-499 — Doxycycline Hyclate, 49999-126 — Doxycycline Hyclate, 50090-4981 — Doxycycline Hyclate, 50090-5380 — doxycycline hyclate, 50090-5560 — doxycycline hyclate, 50090-5588 — doxycycline hyclate, 50090-6212 — Doxycycline hyclate, 50090-7410 — doxycycline, 50090-7411 — doxycycline, 50090-7546 — 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.