NDC product
clindamycin hydrochloride
NDC 69238-2121 · Amneal Pharmaceuticals NY LLC
Key facts
| Product NDC | 69238-2121 |
|---|---|
| Proprietary name | clindamycin hydrochloride |
| Nonproprietary name | clindamycin hydrochloride |
| Substances | CLINDAMYCIN HYDROCHLORIDE |
| Dosage form | CAPSULE, GELATIN COATED |
| Route | ORAL |
| Labeler | Amneal Pharmaceuticals NY LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA065194 |
| Pharmacologic classes | Decreased Sebaceous Gland Activity [PE], Lincosamide Antibacterial [EPC], Lincosamides [CS], Neuromuscular Blockade [PE] |
| Marketing start | Apr 25, 2022 |
| 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: