Home
>
National Drug Code (NDC)
>
Guanidine hydrochloride
Guanidine hydrochloride - 0085-0492-01 - (Guanidine hydrochloride)
Drug Information of Guanidine hydrochloride
| Product NDC: | 0085-0492 |
| Proprietary Name: | Guanidine hydrochloride |
| Non Proprietary Name: | Guanidine hydrochloride |
| Active Ingredient(s): | 125 mg/1 & nbsp; Guanidine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guanidine hydrochloride
| Product NDC: | 0085-0492 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA001546 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19391002 |
Package Information of Guanidine hydrochloride
| Package NDC: | 0085-0492-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0085-0492-01) |
NDC Information of Guanidine hydrochloride
| NDC Code | 0085-0492-01 |
| Proprietary Name | Guanidine hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (0085-0492-01) |
| Product NDC | 0085-0492 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Guanidine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19391002 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | GUANIDINE HYDROCHLORIDE |
| Strength Number | 125 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Acetylcholine Releasing Agent [EPC],Increased Acetylcholine Activity [PE] |
