Prescription drug · UNAPPROVED DRUG OTHER
Phenobarbital NDC 70518-4719
Phenobarbital 16.2 mg/1 · Tablet · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-4719-0 | 70518471900 | 100 POUCH in 1 BOX (70518-4719-0) / 1 TABLET in 1 POUCH (70518-4719-1)Marketed from Aug 3, 2026 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Phenobarbital
- Generic name (nonproprietary)
- phenobarbital
- Active ingredients
- Phenobarbital — 16.2 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- REMEDYREPACK INC.
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- DEA schedule
- CIV
- Identifiers
- Product ID 70518-4719_584bfaea-4219-0259-e063-6294a90ae3dfSPL ID 584bfaea-4219-0259-e063-6294a90ae3dfSPL set ID 3e7637d9-2a8a-4063-8b14-1d1444629a15RxCUI 198086UNII YQE403BP4D
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N470518471900followed by a unit qualifier and the quantityPackage 70518-4719-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE 1. Sedative 2. Anticonvulsant – For the treatment of generalized and partial seizures.
Excerpt only. Read the full label for complete information.