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NUCYNTA
NUCYNTA - 21695-069-72 - (tapentadol hydrochloride)
Drug Information of NUCYNTA
| Product NDC: | 21695-069 |
| Proprietary Name: | NUCYNTA |
| Non Proprietary Name: | tapentadol hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; tapentadol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NUCYNTA
| Product NDC: | 21695-069 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022304 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090601 |
Package Information of NUCYNTA
| Package NDC: | 21695-069-72 |
| Package Description: | 120 TABLET, FILM COATED in 1 BOTTLE (21695-069-72) |
NDC Information of NUCYNTA
| NDC Code | 21695-069-72 |
| Proprietary Name | NUCYNTA |
| Package Description | 120 TABLET, FILM COATED in 1 BOTTLE (21695-069-72) |
| Product NDC | 21695-069 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tapentadol hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090601 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | TAPENTADOL HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
