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Fentanyl
Fentanyl - 49884-762-78 - (Fentanyl)
Drug Information of Fentanyl
| Product NDC: | 49884-762 |
| Proprietary Name: | Fentanyl |
| Non Proprietary Name: | Fentanyl |
| Active Ingredient(s): | 50 ug/h & nbsp; Fentanyl |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fentanyl
| Product NDC: | 49884-762 |
| Labeler Name: | Par Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077062 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070820 |
Package Information of Fentanyl
| Package NDC: | 49884-762-78 |
| Package Description: | 5 POUCH in 1 CARTON (49884-762-78) > 1 PATCH in 1 POUCH (49884-762-52) > 72 h in 1 PATCH |
NDC Information of Fentanyl
| NDC Code | 49884-762-78 |
| Proprietary Name | Fentanyl |
| Package Description | 5 POUCH in 1 CARTON (49884-762-78) > 1 PATCH in 1 POUCH (49884-762-52) > 72 h in 1 PATCH |
| Product NDC | 49884-762 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fentanyl |
| Dosage Form Name | PATCH |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20070820 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc. |
| Substance Name | FENTANYL |
| Strength Number | 50 |
| Strength Unit | ug/h |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
