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Tramadol Hydrochloride
Tramadol Hydrochloride - 10370-222-11 - (Tramadol Hydrochloride)
Drug Information of Tramadol Hydrochloride
| Product NDC: | 10370-222 |
| Proprietary Name: | Tramadol Hydrochloride |
| Non Proprietary Name: | Tramadol Hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; Tramadol Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tramadol Hydrochloride
| Product NDC: | 10370-222 |
| Labeler Name: | Par Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200491 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120627 |
Package Information of Tramadol Hydrochloride
| Package NDC: | 10370-222-11 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-222-11) |
NDC Information of Tramadol Hydrochloride
| NDC Code | 10370-222-11 |
| Proprietary Name | Tramadol Hydrochloride |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-222-11) |
| Product NDC | 10370-222 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tramadol Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120627 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceuticals, Inc. |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
