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ACTIQ
ACTIQ - 63459-506-30 - (fentanyl citrate)
Drug Information of ACTIQ
| Product NDC: | 63459-506 |
| Proprietary Name: | ACTIQ |
| Non Proprietary Name: | fentanyl citrate |
| Active Ingredient(s): | 600 ug/1 & nbsp; fentanyl citrate |
| Administration Route(s): | ORAL; TRANSMUCOSAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACTIQ
| Product NDC: | 63459-506 |
| Labeler Name: | Cephalon, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020747 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19981104 |
Package Information of ACTIQ
| Package NDC: | 63459-506-30 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (63459-506-30) > 3 LOZENGE in 1 BLISTER PACK (63459-506-01) |
NDC Information of ACTIQ
| NDC Code | 63459-506-30 |
| Proprietary Name | ACTIQ |
| Package Description | 10 BLISTER PACK in 1 CARTON (63459-506-30) > 3 LOZENGE in 1 BLISTER PACK (63459-506-01) |
| Product NDC | 63459-506 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fentanyl citrate |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL; TRANSMUCOSAL |
| Start Marketing Date | 19981104 |
| Marketing Category Name | NDA |
| Labeler Name | Cephalon, Inc. |
| Substance Name | FENTANYL CITRATE |
| Strength Number | 600 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
