Prescription drug · UNAPPROVED DRUG OTHER
Phenobarbital NDC 70518-4720
Phenobarbital 97.2 mg/1 · Tablet · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-4720-0 | 70518472000 | 100 POUCH in 1 BOX (70518-4720-0) / 1 TABLET in 1 POUCH (70518-4720-1)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 — 97.2 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- REMEDYREPACK INC.NDC labeler code 70518
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- DEA schedule
- CIV
- Identifiers
- Product ID 70518-4720_5837e1f3-1059-6635-e063-6294a90a5e32SPL ID 5837e1f3-1059-6635-e063-6294a90a5e32SPL set ID b43c3611-24f6-4eaf-ac68-c2807f92ca98RxCUI 199164UNII 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
N470518472000followed by a unit qualifier and the quantityPackage 70518-4720-00. 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 A. Sedative B. Anticonvulsant – For the treatment of generalized and partial seizures.
Excerpt only. Read the full label for complete information.
About NDC 70518-4720
- What is NDC 70518-4720?
- 70518-4720 is the product NDC for Phenobarbital, Phenobarbital 97.2 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. 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?
- REMEDYREPACK INC., NDC labeler code 70518. 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 64.8 mg/1 | TabletOral | Chartwell RX, LLC | 62135-557 | 62135-0557-90 |
| 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 32.4 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4718 | 70518-4718-00 |
| Phenobarbital | Phenobarbital 64.8 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4717 | 70518-4717-00 |