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Estazolam
Estazolam - 49884-112-01 - (Estazolam)
Drug Information of Estazolam
| Product NDC: | 49884-112 |
| Proprietary Name: | Estazolam |
| Non Proprietary Name: | Estazolam |
| Active Ingredient(s): | 1 mg/1 & nbsp; Estazolam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Estazolam
| Product NDC: | 49884-112 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074921 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091204 |
Package Information of Estazolam
| Package NDC: | 49884-112-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (49884-112-01) |
NDC Information of Estazolam
| NDC Code | 49884-112-01 |
| Proprietary Name | Estazolam |
| Package Description | 100 TABLET in 1 BOTTLE (49884-112-01) |
| Product NDC | 49884-112 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Estazolam |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091204 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | ESTAZOLAM |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
