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ZALEPLON
ZALEPLON - 67877-211-10 - (ZALEPLON)
Drug Information of ZALEPLON
| Product NDC: | 67877-211 |
| Proprietary Name: | ZALEPLON |
| Non Proprietary Name: | ZALEPLON |
| Active Ingredient(s): | 10 mg/1 & nbsp; ZALEPLON |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZALEPLON
| Product NDC: | 67877-211 |
| Labeler Name: | Ascend Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078989 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101215 |
Package Information of ZALEPLON
| Package NDC: | 67877-211-10 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE (67877-211-10) |
NDC Information of ZALEPLON
| NDC Code | 67877-211-10 |
| Proprietary Name | ZALEPLON |
| Package Description | 1000 CAPSULE in 1 BOTTLE (67877-211-10) |
| Product NDC | 67877-211 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ZALEPLON |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20101215 |
| Marketing Category Name | ANDA |
| Labeler Name | Ascend Laboratories, LLC |
| Substance Name | ZALEPLON |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | gamma-Aminobutyric Acid A Receptor Agonist [EPC],GABA A Agonists [MoA],Central Nervous System Depression [PE] |
