NDC product
Marbeta 25 Kit
NDC 76420-785 · Asclemed USA, Inc.
Key facts
| Product NDC | 76420-785 |
|---|---|
| Proprietary name | Marbeta 25 Kit |
| Nonproprietary name | Betamethasone Sodium Phosphate and Betamethasone Acetate, Bupivacaine Hydrochloride, Povidine Iodine |
| Dosage form | KIT |
| Route | EPIDURAL, INFILTRATION, INTRA-ARTICULAR, INTRALESIONAL, INTRAMUSCULAR, TOPICAL |
| Labeler | Asclemed USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Apr 28, 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: