Prescription drug · UNAPPROVED DRUG OTHER
Phenobarbital NDC 67296-2145
Phenobarbital 32.4 mg/1 · Tablet · Oral · Redpharm Drug
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 67296-2145-2 | 67296214502 | 20 TABLET in 1 BOTTLE (67296-2145-2)Marketed from Sep 8, 2023 |
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 — 32.4 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Redpharm Drug
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- DEA schedule
- CIV
- Identifiers
- Product ID 67296-2145_4637fbff-2c91-27f6-e063-6394a90a886fSPL ID 4637fbff-2c91-27f6-e063-6394a90a886fSPL set ID 3252a6bb-02e8-7992-e063-6394a90aec3dRxCUI 199167UNII YQE403BP4DUPC 0369367625012, 0369367626019
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
N467296214502followed by a unit qualifier and the quantityPackage 67296-2145-02. 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.