Paclitaxel

NDC 0703-3216 · Teva Parenteral Medicines, Inc.

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic namePaclitaxel

Dosage formINJECTION, SOLUTION, CONCENTRATE

RouteINTRAVENOUS

Active ingredient(s)PACLITAXEL

Strength6 mg/mL

Pharmacologic classMicrotubule Inhibition [PE], Microtubule Inhibitor [EPC]

Marketing categoryANDA

Packages

0703-3216-01 — 1 VIAL, MULTI-DOSE in 1 CARTON (0703-3216-01) / 16.7 mL in 1 VIAL, MULTI-DOSE

0703-3216-81 — 1 VIAL, MULTI-DOSE in 1 CARTON (0703-3216-81) / 16.7 mL in 1 VIAL, MULTI-DOSE

J9267 — Injection, paclitaxel, 1 mg Medicare Part B payment limit (ASP + 6%): $0.11

FDA lists these products with the same active ingredient.

0480-3290 — Paclitaxel, 0517-4300 — Paclitaxel, 0703-3213 — Paclitaxel, 0703-3217 — Paclitaxel, 0703-3218 — Paclitaxel, 0781-3531 — Paclitaxel, 16714-137 — Paclitaxel, 23155-882 — paclitaxel, 23155-883 — paclitaxel, 23155-884 — paclitaxel, 25021-255 — Paclitaxel, 46708-620 — Paclitaxel, 46708-621 — Paclitaxel, 46708-622 — Paclitaxel, 61703-015 — PACLITAXEL, 61703-342 — PACLITAXEL, 62332-620 — Paclitaxel, 62332-621 — Paclitaxel, 62332-622 — Paclitaxel, 63323-763 — Paclitaxel, +20 more

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