NDC product
Diethylpropion Hydrochloride ER
NDC 68071-3837 · NuCare Pharmaceuticals, Inc.
Key facts
| Product NDC | 68071-3837 |
|---|---|
| Proprietary name | Diethylpropion Hydrochloride |
| Nonproprietary name | Diethylpropion Hydrochloride |
| Substances | DIETHYLPROPION HYDROCHLORIDE |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | NuCare Pharmaceuticals, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA091680 |
| DEA schedule | CIV |
| Pharmacologic classes | Appetite Suppression [PE], Increased Sympathetic Activity [PE], Sympathomimetic Amine Anorectic [EPC] |
| Marketing start | Oct 24, 2011 |
| Listing certified through | Dec 31, 2026 |
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: