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Guaifenesin
Guaifenesin - 45802-498-58 - (Guaifenesin)
Drug Information of Guaifenesin
| Product NDC: | 45802-498 |
| Proprietary Name: | Guaifenesin |
| 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 Guaifenesin
| Product NDC: | 45802-498 |
| Labeler Name: | Perrigo New York Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078912 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120328 |
Package Information of Guaifenesin
| Package NDC: | 45802-498-58 |
| Package Description: | 1 BOTTLE in 1 CARTON (45802-498-58) > 40 TABLET, EXTENDED RELEASE in 1 BOTTLE |
NDC Information of Guaifenesin
| NDC Code | 45802-498-58 |
| Proprietary Name | Guaifenesin |
| Package Description | 1 BOTTLE in 1 CARTON (45802-498-58) > 40 TABLET, EXTENDED RELEASE in 1 BOTTLE |
| Product NDC | 45802-498 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120328 |
| Marketing Category Name | ANDA |
| Labeler Name | Perrigo New York Inc |
| Substance Name | GUAIFENESIN |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
