Guaifenesin and Pseudoephedrine Hydrochloride (Guaifenesin and Pseudoephedrine Hydrochloride) — NDC 41415-994 by PUBLIX SUPER MARK
Guaifenesin and Pseudoephedrine Hydrochloride (Guaifenesin and Pseudoephedrine Hydrochloride) — NDC 41415-994 by PUBLIX SUPER MARK is one of 9,000 drug products in the NDCLookup dataset. Key details — Brand name: Guaifenesin and Pseudoephedrine Hydrochloride; Generic name: Guaifenesin and Pseudoephedrine Hydrochloride;
| Brand name | Guaifenesin and Pseudoephedrine Hydrochloride |
|---|---|
| Generic name | Guaifenesin and Pseudoephedrine Hydrochloride |
| Product NDC | 41415-994 |
| Labeler | PUBLIX SUPER MARKETS, INC |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Active ingredients | GUAIFENESIN 600 mg/1; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1 |
| Pharmacologic class | Adrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-Adrenergic Agonist [EPC] |
| Marketing category | ANDA |
| Product type | HUMAN OTC DRUG |
| Source | openFDA NDC Directory |
$899/mo
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