Prescription drug · UNAPPROVED DRUG OTHER
Phenobarbital NDC 69367-367
Phenobarbital 20 mg/5mL · Elixir · Oral · Westminster Pharmaceuticals, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69367-367-16 | 69367036716 | 473 mL in 1 BOTTLE, PLASTIC (69367-367-16)Marketed from May 1, 2025 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 20 mg/5mL
- Dosage form
- Elixir
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- DEA schedule
- CIV
- Identifiers
- Product ID 69367-367_cf0962ad-4f57-4733-a836-844ac7764a01SPL ID cf0962ad-4f57-4733-a836-844ac7764a01SPL set ID 87148299-a3a6-40af-afa6-f32ac2f678c6RxCUI 702519UNII YQE403BP4DUPC 0369367367165
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
N469367036716followed by a unit qualifier and the quantityPackage 69367-0367-16. 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 A. Sedative B. Anticonvulsant- For the treatment of generalized and partial seizures.
Excerpt only. Read the full label for complete information.