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WAL SOM
WAL SOM - 0363-0441-01 - (Doxylamine succinate)
Drug Information of WAL SOM
| Product NDC: | 0363-0441 |
| Proprietary Name: | WAL SOM |
| Non Proprietary Name: | Doxylamine succinate |
| Active Ingredient(s): | 25 mg/1 & nbsp; Doxylamine succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of WAL SOM
| Product NDC: | 0363-0441 |
| Labeler Name: | Walgreen Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA040167 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990305 |
Package Information of WAL SOM
| Package NDC: | 0363-0441-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (0363-0441-01) > 96 TABLET in 1 BOTTLE |
NDC Information of WAL SOM
| NDC Code | 0363-0441-01 |
| Proprietary Name | WAL SOM |
| Package Description | 1 BOTTLE in 1 CARTON (0363-0441-01) > 96 TABLET in 1 BOTTLE |
| Product NDC | 0363-0441 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Doxylamine succinate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19990305 |
| Marketing Category Name | ANDA |
| Labeler Name | Walgreen Company |
| Substance Name | DOXYLAMINE SUCCINATE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
