| Product NDC: | 0363-0950 |
| Proprietary Name: | wal zan 150 |
| 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) |
| Product NDC: | 0363-0950 |
| Labeler Name: | Walgreen Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA091429 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110917 |
| Package NDC: | 0363-0950-04 |
| Package Description: | 1 BOTTLE in 1 CARTON (0363-0950-04) > 85 TABLET, FILM COATED in 1 BOTTLE |
| NDC Code | 0363-0950-04 |
| Proprietary Name | wal zan 150 |
| Package Description | 1 BOTTLE in 1 CARTON (0363-0950-04) > 85 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 0363-0950 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ranitidine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110917 |
| Marketing Category Name | ANDA |
| Labeler Name | Walgreen Company |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |