Product NDC: | 49035-498 |
Proprietary Name: | Equate Mucus ER |
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) |
Product NDC: | 49035-498 |
Labeler Name: | Wal-Mart Stores Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA078912 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130322 |
Package NDC: | 49035-498-60 |
Package Description: | 1 BOTTLE in 1 CARTON (49035-498-60) > 20 TABLET, EXTENDED RELEASE in 1 BOTTLE |
NDC Code | 49035-498-60 |
Proprietary Name | Equate Mucus ER |
Package Description | 1 BOTTLE in 1 CARTON (49035-498-60) > 20 TABLET, EXTENDED RELEASE in 1 BOTTLE |
Product NDC | 49035-498 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20130322 |
Marketing Category Name | ANDA |
Labeler Name | Wal-Mart Stores Inc |
Substance Name | GUAIFENESIN |
Strength Number | 600 |
Strength Unit | mg/1 |
Pharmaceutical Classes |