NDC 80725-005

Valium

Diazepam

Valium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Waylis Therapuetics Llc. The primary component is Diazepam.

Product ID80725-005_dc250376-39ef-2207-e053-2a95a90a4901
NDC80725-005
Product TypeHuman Prescription Drug
Proprietary NameValium
Generic NameDiazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2022-04-04
Marketing CategoryNDA /
Application NumberNDA013263
Labeler NameWaylis Therapuetics LLC
Substance NameDIAZEPAM
Active Ingredient Strength5 mg/1
Pharm ClassesBenzodiazepine [EPC], Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 80725-005-01

100 TABLET in 1 BOTTLE (80725-005-01)
Marketing Start Date2022-04-04
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Valium" or generic name "Diazepam"

NDCBrand NameGeneric Name
0140-0004Valiumdiazepam
0140-0005Valiumdiazepam
0140-0006Valiumdiazepam
55289-117ValiumValium
65084-313ValiumValium
65084-312ValiumValium
80425-0120ValiumValium
0187-0658Diastatdiazepam
0187-0659Diastatdiazepam
0054-3188DiazepamDiazepam
0093-6137DiazepamDiazepam
0093-6138DiazepamDiazepam
0093-6139DiazepamDiazepam
0121-0905DiazepamDiazepam
0172-3925DiazepamDiazepam
0172-3926DiazepamDiazepam
0172-3927DiazepamDiazepam

Trademark Results [Valium]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VALIUM
VALIUM
72122442 0725548 Live/Registered
HOFFMANN-LA ROCHE INC.
1961-06-20

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