NDC 72319-006

Selegiline Hydrochloride

Selegiline Hydrochloride

Selegiline Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by I3 Pharmaceuticals, Llc. The primary component is Selegiline Hydrochloride.

Product ID72319-006_c81e983b-455e-2e65-e053-2a95a90a3123
NDC72319-006
Product TypeHuman Prescription Drug
Proprietary NameSelegiline Hydrochloride
Generic NameSelegiline Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2021-07-30
Marketing CategoryANDA /
Application NumberANDA074672
Labeler Namei3 Pharmaceuticals, LLC
Substance NameSELEGILINE HYDROCHLORIDE
Active Ingredient Strength5 mg/1
Pharm ClassesMonoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA],Monoamine Oxidase Type B Inhibitor [EPC],Monoamine Oxidase-B Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 72319-006-02

60 TABLET in 1 BOTTLE (72319-006-02)
Marketing Start Date2021-07-30
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Selegiline Hydrochloride" or generic name "Selegiline Hydrochloride"

NDCBrand NameGeneric Name
0378-9290Selegiline Hydrochlorideselegiline hydrochloride
10135-737Selegiline HydrochlorideSelegiline Hydrochloride
16571-659Selegiline HydrochlorideSelegiline Hydrochloride
50090-2918Selegiline HydrochlorideSelegiline Hydrochloride
51862-146Selegiline HydrochlorideSelegiline Hydrochloride
60429-019SELEGILINE HYDROCHLORIDESELEGILINE HYDROCHLORIDE
60429-176Selegiline HydrochlorideSelegiline Hydrochloride
60505-0055SELEGILINE HYDROCHLORIDESELEGILINE HYDROCHLORIDE
60505-3438Selegiline HydrochlorideSelegiline Hydrochloride
67253-700SELEGILINE HYDROCHLORIDESELEGILINE HYDROCHLORIDE
68151-2649SELEGILINE HYDROCHLORIDESELEGILINE HYDROCHLORIDE
70954-504Selegiline HydrochlorideSelegiline Hydrochloride
71205-888Selegiline HydrochlorideSelegiline Hydrochloride
72319-006Selegiline HydrochlorideSelegiline Hydrochloride
0187-0453ZELAPARSELEGILINE HYDROCHLORIDE

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