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DOXYCYCLINE HYCLATE

NDC 23155-141 · Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Generic namedoxycycline hyclate
Dosage formTABLET, DELAYED RELEASE
RouteORAL
Active ingredient(s)DOXYCYCLINE HYCLATE
Strength75 mg/1
Pharmacologic classTetracycline-class Drug [EPC], Tetracyclines [CS]
Marketing categoryANDA

Packages

23155-141-01 — 100 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-141-01)

23155-141-05 — 500 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-141-05)

23155-141-06 — 60 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-141-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0143-9802 — Doxycycline Hyclate, 0143-9803 — Doxycycline Hyclate, 0404-9855 — doxycycline, 0591-4550 — Doxycycline Hyclate, 0591-4575 — Doxycycline Hyclate, 0591-5553 — Doxycycline Hyclate, 0615-8529 — Doxycycline Hyclate, 0904-0428 — Doxycycline Hyclate, 0904-0430 — Doxycycline hyclate, 16110-601 — doxycycline hyclate, 23155-142 — doxycycline hyclate, 23155-143 — doxycycline hyclate, 23155-611 — doxycycline hyclate, 24658-310 — Doxycycline Hyclate, 27241-140 — Doxycycline Hyclate, 27241-141 — Doxycycline Hyclate, 27241-153 — Doxycycline hyclate, 27241-154 — Doxycycline hyclate, 27808-233 — doxycycline, 27808-234 — 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.