Prescription drug · UNAPPROVED DRUG OTHER
Phenobarbital NDC 67046-0059
Phenobarbital 32.4 mg/1 · Tablet · Oral · Coupler LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 67046-0059-3 | 67046005903 | 30 TABLET in 1 BLISTER PACK (67046-0059-3)Marketed from Jun 22, 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 — 32.4 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Coupler LLCNDC labeler code 67046
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- DEA schedule
- CIV
- Identifiers
- Product ID 67046-0059_54d790cd-229f-1dbc-e063-6394a90a1ff2SPL ID 54d790cd-229f-1dbc-e063-6394a90a1ff2SPL set ID 54d7915f-4aef-79a1-e063-6294a90aa6efRxCUI 199167UNII 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
N467046005903followed by a unit qualifier and the quantityPackage 67046-0059-03. 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.
About NDC 67046-0059
- What is NDC 67046-0059?
- 67046-0059 is the product NDC for Phenobarbital, Phenobarbital 32.4 mg/1 tablet, listed with the FDA by Coupler LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Phenobarbital.
- What is the active ingredient?
- Phenobarbital.
- Who is the labeler?
- Coupler LLC, NDC labeler code 67046. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Phenobarbital?
- 157 other product NDCs are listed under this name. See all Phenobarbital NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Phenobarbital products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Phenobarbital | Phenobarbital 15 mg/1 | TabletOral | Chartwell RX, LLC | 62135-510 | 62135-0510-90 |
| Phenobarbital | Phenobarbital 30 mg/1 | TabletOral | Chartwell RX, LLC | 62135-514 | 62135-0514-90 |
| Phenobarbital | Phenobarbital 60 mg/1 | TabletOral | Chartwell RX, LLC | 62135-515 | 62135-0515-90 |
| Phenobarbital | Phenobarbital 100 mg/1 | TabletOral | Chartwell RX, LLC | 62135-519 | 62135-0519-90 |
| Phenobarbital | Phenobarbital 16.2 mg/1 | TabletOral | Chartwell RX, LLC | 62135-539 | 62135-0539-90 |
| Phenobarbital | Phenobarbital 32.4 mg/1 | TabletOral | Chartwell RX, LLC | 62135-554 | 62135-0554-90 |
| Phenobarbital | Phenobarbital 97.2 mg/1 | TabletOral | Chartwell RX, LLC | 62135-558 | 62135-0558-90 |
| Phenobarbital | Phenobarbital 64.8 mg/1 | TabletOral | Chartwell RX, LLC | 62135-557 | 62135-0557-90 |
| Phenobarbital | Phenobarbital 16.2 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4719 | 70518-4719-00 |
| Phenobarbital | Phenobarbital 64.8 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4717 | 70518-4717-00 |