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Immediate Release Mucus Relief
Immediate Release Mucus Relief - 21130-555-01 - (Guaifenesin)
Drug Information of Immediate Release Mucus Relief
| Product NDC: | 21130-555 |
| Proprietary Name: | Immediate Release Mucus Relief |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 400 mg/1 & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Immediate Release Mucus Relief
| Product NDC: | 21130-555 |
| Labeler Name: | Safeway |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20051222 |
Package Information of Immediate Release Mucus Relief
| Package NDC: | 21130-555-01 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (21130-555-01) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Immediate Release Mucus Relief
| NDC Code | 21130-555-01 |
| Proprietary Name | Immediate Release Mucus Relief |
| Package Description | 3 BLISTER PACK in 1 CARTON (21130-555-01) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 21130-555 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20051222 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Safeway |
| Substance Name | GUAIFENESIN |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
