NDC 50090-1057

Mirtazapine

Mirtazapine

Mirtazapine is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Mirtazapine.

Product ID50090-1057_d395de56-30b0-499f-93f6-116e1fd8c26c
NDC50090-1057
Product TypeHuman Prescription Drug
Proprietary NameMirtazapine
Generic NameMirtazapine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2009-08-17
Marketing CategoryANDA /
Application NumberANDA076921
Labeler NameA-S Medication Solutions
Substance NameMIRTAZAPINE
Active Ingredient Strength30 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 50090-1057-0

30 TABLET, FILM COATED in 1 BOTTLE (50090-1057-0)
Marketing Start Date2014-11-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-1057-2 [50090105702]

Mirtazapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-01-29
Marketing End Date2019-01-29

NDC 50090-1057-0 [50090105700]

Mirtazapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-01-29
Marketing End Date2019-01-29

NDC 50090-1057-1 [50090105701]

Mirtazapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-01-29
Marketing End Date2019-01-29

NDC 50090-1057-3 [50090105703]

Mirtazapine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-01-29
Marketing End Date2019-01-29

Drug Details

NDC Crossover Matching brand name "Mirtazapine" or generic name "Mirtazapine"

NDCBrand NameGeneric Name
0093-7206MirtazapineMirtazapine
0093-7207MirtazapineMirtazapine
0093-7208MirtazapineMirtazapine
0115-1653MirtazapineMirtazapine
0115-1654MirtazapineMirtazapine
0115-1656MirtazapineMirtazapine
0185-0020mirtazapinemirtazapine
68071-1716MirtazapineMirtazapine
68071-1659MirtazapineMirtazapine
68071-4045MirtazapineMirtazapine
68071-4003MirtazapineMirtazapine
68071-4295MirtazapineMirtazapine
68071-4239MirtazapineMirtazapine
68071-4379MirtazapineMirtazapine
68071-4752MirtazapineMirtazapine
68071-4539MirtazapineMirtazapine
68084-121MirtazapineMirtazapine
68084-120MirtazapineMirtazapine
68084-119MirtazapineMirtazapine
68382-679mirtazapinemirtazapine
68382-676mirtazapinemirtazapine
68382-677mirtazapinemirtazapine
68788-7196MirtazapineMirtazapine
68788-7172MirtazapineMirtazapine
68788-7251MirtazapineMirtazapine
68788-9981MirtazapineMirtazapine
0591-1117MirtazapineMirtazapine
0591-1118MirtazapineMirtazapine
70518-0101MirtazapineMirtazapine
70518-0180MirtazapineMirtazapine
0591-1119MirtazapineMirtazapine
0591-2470MirtazapineMirtazapine
70518-0316MirtazapineMirtazapine
70518-0102MirtazapineMirtazapine
70518-0276MirtazapineMirtazapine
70518-0901MirtazapineMirtazapine
70518-0977MirtazapineMirtazapine
70518-1397MirtazapineMirtazapine
70518-1352MirtazapineMirtazapine
70518-1309MirtazapineMirtazapine
70518-1293MirtazapineMirtazapine
70518-1838MirtazapineMirtazapine
70518-1583MirtazapineMirtazapine
70771-1072mirtazapinemirtazapine
70771-1073mirtazapinemirtazapine
70771-1074mirtazapinemirtazapine
71335-0441MirtazapineMirtazapine
71335-0286MirtazapineMirtazapine
71335-0372MirtazapineMirtazapine
71335-0717MirtazapineMirtazapine

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.