NDC product
POWDER · Zhejiang Syncotide Bio-pharmaceutical Co., Ltd
NDC 14799-0213 · Zhejiang Syncotide Bio-pharmaceutical Co., Ltd
Key facts
| Product NDC | 14799-0213 |
|---|---|
| Nonproprietary name | Bupropion Hydrochloride |
| Substances | BUPROPION HYDROCHLORIDE |
| Dosage form | POWDER |
| Labeler | Zhejiang Syncotide Bio-pharmaceutical Co., Ltd |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Sep 15, 2010 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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: