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mucus relief
mucus relief - 37808-498-60 - (Guaifenesin)
Drug Information of mucus relief
| Product NDC: | 37808-498 |
| Proprietary Name: | mucus relief |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 600 mg/1 & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of mucus relief
| Product NDC: | 37808-498 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078912 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130319 |
Package Information of mucus relief
| Package NDC: | 37808-498-60 |
| Package Description: | 1 BOTTLE in 1 CARTON (37808-498-60) > 20 TABLET, EXTENDED RELEASE in 1 BOTTLE |
NDC Information of mucus relief
| NDC Code | 37808-498-60 |
| Proprietary Name | mucus relief |
| Package Description | 1 BOTTLE in 1 CARTON (37808-498-60) > 20 TABLET, EXTENDED RELEASE in 1 BOTTLE |
| Product NDC | 37808-498 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130319 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | GUAIFENESIN |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
