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ALPRAZOLAM EXTENDED-RELEASE
ALPRAZOLAM EXTENDED-RELEASE - 64980-141-10 - (ALPRAZOLAM)
Drug Information of ALPRAZOLAM EXTENDED-RELEASE
| Product NDC: | 64980-141 |
| Proprietary Name: | ALPRAZOLAM EXTENDED-RELEASE |
| Non Proprietary Name: | ALPRAZOLAM |
| Active Ingredient(s): | 1 mg/1 & nbsp; ALPRAZOLAM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ALPRAZOLAM EXTENDED-RELEASE
| Product NDC: | 64980-141 |
| Labeler Name: | Rising Pharmaceuticals Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077996 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070328 |
Package Information of ALPRAZOLAM EXTENDED-RELEASE
| Package NDC: | 64980-141-10 |
| Package Description: | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-141-10) |
NDC Information of ALPRAZOLAM EXTENDED-RELEASE
| NDC Code | 64980-141-10 |
| Proprietary Name | ALPRAZOLAM EXTENDED-RELEASE |
| Package Description | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64980-141-10) |
| Product NDC | 64980-141 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ALPRAZOLAM |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20070328 |
| Marketing Category Name | ANDA |
| Labeler Name | Rising Pharmaceuticals Inc |
| Substance Name | ALPRAZOLAM |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
