NDC Labeler Be Pharmaceuticals Inc.

Be Pharmaceuticals Inc. labeler's code is 71839. The labeler has 13 products that have an assigned National Drug Code.

NDC	Proprietary Name	Non-Proprietary Name	Dosage Form	Route Name	Product Type	Status
71839-104	Fosaprepitant	Fosaprepitant	Injection, Powder, Lyophilized, For Solution	Intravenous	Human Prescription Drug	ACTIVE
71839-105	Neostigmine Methylsulfate	Neostigmine Methylsulfate	Injection	Intravenous	Human Prescription Drug	ACTIVE
71839-106	Neostigmine Methylsulfate	Neostigmine Methylsulfate	Injection	Intravenous	Human Prescription Drug	ACTIVE
71839-107	Daptomycin	Daptomycin	Injection, Powder, Lyophilized, For Solution	Intravenous	Human Prescription Drug	ACTIVE
71839-108	Daptomycin	Daptomycin	Injection, Powder, Lyophilized, For Solution	Intravenous	Human Prescription Drug	ACTIVE
71839-117	Heparin Sodium	Heparin Sodium	Injection, Solution	Intravenous; Subcutaneous	Human Prescription Drug	ACTIVE
71839-118	Heparin Sodium	Heparin Sodium	Injection, Solution	Intravenous; Subcutaneous	Human Prescription Drug	ACTIVE
71839-120	Sodium Nitroprusside	Sodium Nitroprusside	Injection	Intravenous	Human Prescription Drug	ACTIVE
71839-122	Pantoprazole Sodium	Pantoprazole Sodium	Injection, Powder, For Solution	Intravenous	Human Prescription Drug	ACTIVE
71839-123	Glycopyrrolate	Glycopyrrolate	Injection	Intramuscular; Intravenous	Human Prescription Drug	ACTIVE
71839-124	Glycopyrrolate	Glycopyrrolate	Injection	Intramuscular; Intravenous	Human Prescription Drug	ACTIVE
71839-125	Glycopyrrolate	Glycopyrrolate	Injection	Intramuscular; Intravenous	Human Prescription Drug	ACTIVE
71839-126	Glycopyrrolate	Glycopyrrolate	Injection	Intramuscular; Intravenous	Human Prescription Drug	ACTIVE