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Prochlorperazine Edisylate

NDC 70069-371 · Somerset Therapeutics, LLC

Generic nameProchlorperazine Edisylate
Dosage formINJECTION
RouteINTRAMUSCULAR, INTRAVENOUS
Active ingredient(s)PROCHLORPERAZINE EDISYLATE
Strength5 mg/mL
Pharmacologic classPhenothiazine [EPC], Phenothiazines [CS]
Marketing categoryANDA

Packages

70069-371-25 — 25 VIAL in 1 CARTON (70069-371-25) / 2 mL in 1 VIAL (70069-371-01)

Billed under HCPCS

J0780 — Injection, prochlorperazine, up to 10 mg Medicare Part B payment limit (ASP + 6%): $2.76

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0641-6135 — Prochlorperazine Edisylate, 0713-0351 — Prochlorperazine Edisylate, 23155-294 — Prochlorperazine Edisylate, 23155-523 — Prochlorperazine Edisylate, 25021-790 — PROCHLORPERAZINE EDISYLATE, 43066-090 — prochlorperazine edisylate, 51662-1558 — PROCHLORPERAZINE EDISYLATE, 55150-360 — Prochlorperazine Edisylate, 55154-4183 — Prochlorperazine Edisylate, 65145-119 — Prochlorperazine Edisylate, 67457-640 — prochlorperazine edisylate, 68083-435 — Prochlorperazine Edisylate, 68083-436 — Prochlorperazine Edisylate, 70121-1580 — prochlorperazine edisylate, 72266-204 — Prochlorperazine Edisylate, 72572-580 — Prochlorperazine Edisylate, 83634-778 — prochlorperazine edisylate

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