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CYPROHEPTADINE HYDROCHLORIDE
CYPROHEPTADINE HYDROCHLORIDE - 60258-850-10 - (CYPROHEPTADINE HYDROCHLORIDE)
Drug Information of CYPROHEPTADINE HYDROCHLORIDE
| Product NDC: | 60258-850 |
| 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: | 60258-850 |
| Labeler Name: | Cypress Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040644 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100615 |
Package Information of CYPROHEPTADINE HYDROCHLORIDE
| Package NDC: | 60258-850-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (60258-850-10) |
NDC Information of CYPROHEPTADINE HYDROCHLORIDE
| NDC Code | 60258-850-10 |
| Proprietary Name | CYPROHEPTADINE HYDROCHLORIDE |
| Package Description | 1000 TABLET in 1 BOTTLE (60258-850-10) |
| Product NDC | 60258-850 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CYPROHEPTADINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100615 |
| Marketing Category Name | ANDA |
| Labeler Name | Cypress Pharmaceutical, Inc. |
| Substance Name | CYPROHEPTADINE HYDROCHLORIDE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
