Prescription drug · UNAPPROVED DRUG OTHER
Phenobarbital NDC 71205-850
Phenobarbital 97.2 mg/1 · Tablet · Oral · Proficient Rx LP
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71205-850-00 | 71205085000 | 100 TABLET in 1 BOTTLE (71205-850-00)Marketed from Feb 13, 2023 | |
| 71205-850-11 | 71205085011 | 1000 TABLET in 1 BOTTLE (71205-850-11)Marketed from Feb 13, 2023 | |
| 71205-850-30 | 71205085030 | 30 TABLET in 1 BOTTLE (71205-850-30)Marketed from Feb 13, 2023 | |
| 71205-850-55 | 71205085055 | 500 TABLET in 1 BOTTLE (71205-850-55)Marketed from Feb 13, 2023 | |
| 71205-850-60 | 71205085060 | 60 TABLET in 1 BOTTLE (71205-850-60)Marketed from Feb 13, 2023 | |
| 71205-850-64 | 71205085064 | 240 TABLET in 1 BOTTLE (71205-850-64)Marketed from Feb 13, 2023 | |
| 71205-850-72 | 71205085072 | 120 TABLET in 1 BOTTLE (71205-850-72)Marketed from Feb 13, 2023 | |
| 71205-850-78 | 71205085078 | 180 TABLET in 1 BOTTLE (71205-850-78)Marketed from Feb 13, 2023 | |
| 71205-850-90 | 71205085090 | 90 TABLET in 1 BOTTLE (71205-850-90)Marketed from Feb 13, 2023 |
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 — 97.2 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Proficient Rx LP
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- DEA schedule
- CIV
- Identifiers
- Product ID 71205-850_47b5e7d0-f031-4f6c-a496-c92f9f972f53SPL ID 47b5e7d0-f031-4f6c-a496-c92f9f972f53SPL set ID 47b5e7d0-f031-4f6c-a496-c92f9f972f53RxCUI 198086, 199164, 199167, 199168UNII YQE403BP4DUPC 0371205847302, 0371205849306, 0371205850302, 0371205846305
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
N471205085000followed by a unit qualifier and the quantityPackage 71205-0850-00. 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.