| Product NDC: | 37808-441 |
| Proprietary Name: | Sleep Aid |
| 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) |
| Product NDC: | 37808-441 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA040167 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980506 |
| Package NDC: | 37808-441-64 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (37808-441-64) > 16 TABLET in 1 BLISTER PACK |
| NDC Code | 37808-441-64 |
| Proprietary Name | Sleep Aid |
| Package Description | 2 BLISTER PACK in 1 CARTON (37808-441-64) > 16 TABLET in 1 BLISTER PACK |
| Product NDC | 37808-441 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Doxylamine succinate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19980506 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | DOXYLAMINE SUCCINATE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |