Home
>
National Drug Code (NDC)
>
berkley and jensen acid reducer
berkley and jensen acid reducer - 68391-950-01 - (Ranitidine)
Drug Information of berkley and jensen acid reducer
| Product NDC: | 68391-950 |
| Proprietary Name: | berkley and jensen acid reducer |
| Non Proprietary Name: | Ranitidine |
| Active Ingredient(s): | 150 mg/1 & nbsp; Ranitidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of berkley and jensen acid reducer
| Product NDC: | 68391-950 |
| Labeler Name: | BJWC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091429 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120203 |
Package Information of berkley and jensen acid reducer
| Package NDC: | 68391-950-01 |
| Package Description: | 2 BOTTLE in 1 PACKAGE (68391-950-01) > 95 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of berkley and jensen acid reducer
| NDC Code | 68391-950-01 |
| Proprietary Name | berkley and jensen acid reducer |
| Package Description | 2 BOTTLE in 1 PACKAGE (68391-950-01) > 95 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 68391-950 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ranitidine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120203 |
| Marketing Category Name | ANDA |
| Labeler Name | BJWC |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
