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ALPRAZOLAM
ALPRAZOLAM - 52959-965-30 - (ALPRAZOLAM)
Drug Information of ALPRAZOLAM
| Product NDC: | 52959-965 |
| Proprietary Name: | ALPRAZOLAM |
| 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
| Product NDC: | 52959-965 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077996 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070328 |
Package Information of ALPRAZOLAM
| Package NDC: | 52959-965-30 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (52959-965-30) |
NDC Information of ALPRAZOLAM
| NDC Code | 52959-965-30 |
| Proprietary Name | ALPRAZOLAM |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (52959-965-30) |
| Product NDC | 52959-965 |
| 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 | H.J. Harkins Company, Inc. |
| Substance Name | ALPRAZOLAM |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
