| NDC Code | 69729-222-06 |
|---|
| Package Description | 3 POUCH in 1 CARTON (69729-222-06) / 2 TABLET in 1 POUCH |
|---|
| Product NDC | 69729-222 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl |
|---|
| Non-Proprietary Name | Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hcl |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190826 |
|---|
| Marketing Category Name | OTC MONOGRAPH FINAL |
|---|
| Application Number | part341 |
|---|
| Manufacturer | OPMX LLC |
|---|
| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
|---|
| Strength | 500; 4; 10 |
|---|
| Strength Unit | mg/1; mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC] |
|---|