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Neostigmine methylsulfate

NDC 71839-106 · BE Pharmaceuticals Inc.

Generic nameNeostigmine methylsulfate
Dosage formINJECTION
RouteINTRAVENOUS
Active ingredient(s)NEOSTIGMINE METHYLSULFATE
Strength1 mg/mL
Pharmacologic classCholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
Marketing categoryANDA

Packages

71839-106-10 — 10 VIAL, MULTI-DOSE in 1 CARTON (71839-106-10) / 10 mL in 1 VIAL, MULTI-DOSE

71839-106-24 — 24 CARTON in 1 CARTON (71839-106-24) / 1 VIAL, MULTI-DOSE in 1 CARTON (71839-106-01) / 10 mL in 1 VIAL, MULTI-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70069-805 — Neostigmine Methylsulfate, 70069-806 — Neostigmine Methylsulfate, 70121-1478 — Neostigmine methylsulfate, 70121-1479 — Neostigmine methylsulfate, 70594-069 — Neostigmine Methylsulfate, 70594-072 — Neostigmine Methylsulfate, 70700-171 — Neostigmine methylsulfate, 70700-172 — Neostigmine methylsulfate, 71288-500 — neostigmine methylsulfate, 71288-501 — neostigmine methylsulfate, 71839-105 — Neostigmine methylsulfate, 71872-7016 — NEOSTIGMINE METHYLSULFATE, 71872-7143 — neostigmine methylsulfate, 71872-7178 — Neostigmine, 71872-7271 — Neostigmine Methylsulfate, 71872-7322 — NEOSTIGMINE METHYLSULFATE, 72572-462 — Neostigmine Methylsulfate, 76045-214 — Neostigmine Methylsulfate, 76045-383 — Neostigmine Methylsulfate, 84549-172 — Neostigmine methylsulfate, +32 more

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