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Docetaxel

NDC 46708-678 · Alembic Pharmaceuticals Limited

Generic nameDocetaxel
Dosage formINJECTION
RouteINTRAVENOUS
Active ingredient(s)DOCETAXEL ANHYDROUS
Strength10 mg/mL
Pharmacologic classMicrotubule Inhibition [PE], Microtubule Inhibitor [EPC]
Marketing categoryANDA

Packages

46708-678-02 — 1 VIAL, SINGLE-DOSE in 1 CARTON (46708-678-02) / 2 mL in 1 VIAL, SINGLE-DOSE

46708-678-08 — 1 VIAL, MULTI-DOSE in 1 CARTON (46708-678-08) / 8 mL in 1 VIAL, MULTI-DOSE

46708-678-16 — 1 VIAL, MULTI-DOSE in 1 CARTON (46708-678-16) / 16 mL in 1 VIAL, MULTI-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0409-0201 — DOCETAXEL ANHYDROUS, 0409-1732 — DOCETAXEL ANHYDROUS, 0409-2026 — DOCETAXEL ANHYDROUS, 0409-7870 — DOCETAXEL ANHYDROUS, 16729-267 — docetaxel, 25021-245 — Docetaxel Anhydrous, 25021-254 — Docetaxel Anhydrous, 43066-044 — Docetaxel, 43066-046 — Docetaxel, 43066-048 — Docetaxel, 47335-323 — Docetaxel, 47335-895 — Docetaxel, 47335-939 — Docetaxel, 55150-378 — Docetaxel, 55150-379 — Docetaxel, 55150-380 — Docetaxel, 62332-678 — Docetaxel, 67457-531 — DOCETAXEL ANHYDROUS, 67457-532 — DOCETAXEL ANHYDROUS, 67457-533 — DOCETAXEL ANHYDROUS, +15 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.