Home
>
National Drug Code (NDC)
>
CYPROHEPTADINE HYDROCHLORIDE
CYPROHEPTADINE HYDROCHLORIDE - 52125-014-02 - (CYPROHEPTADINE HYDROCHLORIDE)
Drug Information of CYPROHEPTADINE HYDROCHLORIDE
| Product NDC: | 52125-014 |
| Proprietary Name: | CYPROHEPTADINE HYDROCHLORIDE |
| Non Proprietary Name: | CYPROHEPTADINE HYDROCHLORIDE |
| Active Ingredient(s): | 4 mg/1 & nbsp; CYPROHEPTADINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CYPROHEPTADINE HYDROCHLORIDE
| Product NDC: | 52125-014 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087056 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120816 |
Package Information of CYPROHEPTADINE HYDROCHLORIDE
| Package NDC: | 52125-014-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (52125-014-02) |
NDC Information of CYPROHEPTADINE HYDROCHLORIDE
| NDC Code | 52125-014-02 |
| Proprietary Name | CYPROHEPTADINE HYDROCHLORIDE |
| Package Description | 30 TABLET in 1 BLISTER PACK (52125-014-02) |
| Product NDC | 52125-014 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CYPROHEPTADINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120816 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | CYPROHEPTADINE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
