Product NDC: | 51079-286 |
Proprietary Name: | Diazepam |
Non Proprietary Name: | diazepam |
Active Ingredient(s): | 10 mg/1 & nbsp; diazepam |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51079-286 |
Labeler Name: | UDL Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070325 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091120 |
Package NDC: | 51079-286-20 |
Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-286-20) > 1 TABLET in 1 BLISTER PACK (51079-286-01) |
NDC Code | 51079-286-20 |
Proprietary Name | Diazepam |
Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-286-20) > 1 TABLET in 1 BLISTER PACK (51079-286-01) |
Product NDC | 51079-286 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | diazepam |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20091120 |
Marketing Category Name | ANDA |
Labeler Name | UDL Laboratories, Inc. |
Substance Name | DIAZEPAM |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |