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naltrexone hydrochloride
naltrexone hydrochloride - 0185-0039-01 - (naltrexone hydrochloride)
Drug Information of naltrexone hydrochloride
| Product NDC: | 0185-0039 |
| 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: | 0185-0039 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075434 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000308 |
Package Information of naltrexone hydrochloride
| Package NDC: | 0185-0039-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0185-0039-01) |
NDC Information of naltrexone hydrochloride
| NDC Code | 0185-0039-01 |
| Proprietary Name | naltrexone hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0185-0039-01) |
| Product NDC | 0185-0039 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | naltrexone hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20000308 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | NALTREXONE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
