NDC product
Guaifenesin and Pseudoephedrine HCl
NDC 62207-828 · Granules India Ltd
Key facts
| Product NDC | 62207-828 |
|---|---|
| Proprietary name | Guaifenesin and Pseudoephedrine HCl |
| Nonproprietary name | Guaifenesin and Pseudoephedrine HCl |
| Substances | GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | Granules India Ltd |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA216082 |
| Pharmacologic classes | Adrenergic alpha-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-Adrenergic Agonist [EPC] |
| Marketing start | Jun 1, 2023 |
| Listing certified through | Dec 31, 2027 |
At a glance
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About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: