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Fentanyl buccal
Fentanyl buccal - 0591-3572-96 - (Fentanyl buccal)
Drug Information of Fentanyl buccal
| Product NDC: | 0591-3572 |
| Proprietary Name: | Fentanyl buccal |
| Non Proprietary Name: | Fentanyl buccal |
| Active Ingredient(s): | 200 ug/1 & nbsp; Fentanyl buccal |
| Administration Route(s): | BUCCAL; ORAL; TRANSMUCOSAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fentanyl buccal
| Product NDC: | 0591-3572 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079075 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110107 |
Package Information of Fentanyl buccal
| Package NDC: | 0591-3572-96 |
| Package Description: | 7 BLISTER PACK in 1 CARTON (0591-3572-96) > 4 TABLET in 1 BLISTER PACK (0591-3572-04) |
NDC Information of Fentanyl buccal
| NDC Code | 0591-3572-96 |
| Proprietary Name | Fentanyl buccal |
| Package Description | 7 BLISTER PACK in 1 CARTON (0591-3572-96) > 4 TABLET in 1 BLISTER PACK (0591-3572-04) |
| Product NDC | 0591-3572 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fentanyl buccal |
| Dosage Form Name | TABLET |
| Route Name | BUCCAL; ORAL; TRANSMUCOSAL |
| Start Marketing Date | 20110107 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | FENTANYL CITRATE |
| Strength Number | 200 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
