| NDC Code | 57344-136-02 |
|---|
| Package Description | 2 BLISTER PACK in 1 CARTON (57344-136-02) > 12 TABLET, COATED in 1 BLISTER PACK |
|---|
| Product NDC | 57344-136 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
|---|
| Non-Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride |
|---|
| Dosage Form | TABLET, COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20121228 |
|---|
| Marketing Category Name | OTC MONOGRAPH FINAL |
|---|
| Application Number | part341 |
|---|
| Manufacturer | AAA Pharmaceutical, Inc. |
|---|
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 325; 10; 200; 5 |
|---|
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
|---|