NDC product
Fluoxetine hydrochloride
NDC 43598-632 · Dr. Reddy's Laboratories Inc.
Key facts
| Product NDC | 43598-632 |
|---|---|
| Proprietary name | Fluoxetine hydrochloride |
| Nonproprietary name | Fluoxetine hydrochloride |
| Substances | FLUOXETINE HYDROCHLORIDE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Dr. Reddy's Laboratories Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA211721 |
| Pharmacologic classes | Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA] |
| Marketing start | Jan 28, 2019 |
| 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: