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Naltrexone Hydrochloride
Naltrexone Hydrochloride - 0555-0902-10 - (Naltrexone Hydrochloride)
Drug Information of Naltrexone Hydrochloride
| Product NDC: | 0555-0902 |
| Proprietary Name: | Naltrexone Hydrochloride |
| Non Proprietary Name: | Naltrexone Hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; Naltrexone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naltrexone Hydrochloride
| Product NDC: | 0555-0902 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074918 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980508 |
Package Information of Naltrexone Hydrochloride
| Package NDC: | 0555-0902-10 |
| Package Description: | 50 TABLET, FILM COATED in 1 BOTTLE (0555-0902-10) |
NDC Information of Naltrexone Hydrochloride
| NDC Code | 0555-0902-10 |
| Proprietary Name | Naltrexone Hydrochloride |
| Package Description | 50 TABLET, FILM COATED in 1 BOTTLE (0555-0902-10) |
| Product NDC | 0555-0902 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Naltrexone Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19980508 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | NALTREXONE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
