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Amitriptyline Hydrochloride
Amitriptyline Hydrochloride - 51138-002-30 - (Amitriptyline Hydrochloride)
Drug Information of Amitriptyline Hydrochloride
| Product NDC: | 51138-002 |
| Proprietary Name: | Amitriptyline Hydrochloride |
| Non Proprietary Name: | Amitriptyline Hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; Amitriptyline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amitriptyline Hydrochloride
| Product NDC: | 51138-002 |
| Labeler Name: | Med-Health Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085966 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110101 |
Package Information of Amitriptyline Hydrochloride
| Package NDC: | 51138-002-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (51138-002-30) |
NDC Information of Amitriptyline Hydrochloride
| NDC Code | 51138-002-30 |
| Proprietary Name | Amitriptyline Hydrochloride |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (51138-002-30) |
| Product NDC | 51138-002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amitriptyline Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110101 |
| Marketing Category Name | ANDA |
| Labeler Name | Med-Health Pharma, LLC |
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
