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Fentanyl Citrate
Fentanyl Citrate - 54868-6025-0 - (fentanyl citrate)
Drug Information of Fentanyl Citrate
| Product NDC: | 54868-6025 |
| Proprietary Name: | Fentanyl Citrate |
| Non Proprietary Name: | fentanyl citrate |
| Active Ingredient(s): | 200 ug/1 & nbsp; fentanyl citrate |
| Administration Route(s): | ORAL; TRANSMUCOSAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fentanyl Citrate
| Product NDC: | 54868-6025 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020747 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090424 |
Package Information of Fentanyl Citrate
| Package NDC: | 54868-6025-0 |
| Package Description: | 30 BLISTER PACK in 1 CARTON (54868-6025-0) > 1 LOZENGE in 1 BLISTER PACK |
NDC Information of Fentanyl Citrate
| NDC Code | 54868-6025-0 |
| Proprietary Name | Fentanyl Citrate |
| Package Description | 30 BLISTER PACK in 1 CARTON (54868-6025-0) > 1 LOZENGE in 1 BLISTER PACK |
| Product NDC | 54868-6025 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fentanyl citrate |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL; TRANSMUCOSAL |
| Start Marketing Date | 20090424 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | FENTANYL CITRATE |
| Strength Number | 200 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
