Phenobarbital NDC 71205-849

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-849Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0849Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
71205-849-00	71205084900	100 TABLET in 1 BOTTLE (71205-849-00)Marketed from Feb 13, 2023
71205-849-11	71205084911	1000 TABLET in 1 BOTTLE (71205-849-11)Marketed from Feb 13, 2023
71205-849-30	71205084930	30 TABLET in 1 BOTTLE (71205-849-30)Marketed from Feb 13, 2023
71205-849-55	71205084955	500 TABLET in 1 BOTTLE (71205-849-55)Marketed from Feb 13, 2023
71205-849-60	71205084960	60 TABLET in 1 BOTTLE (71205-849-60)Marketed from Feb 13, 2023
71205-849-64	71205084964	240 TABLET in 1 BOTTLE (71205-849-64)Marketed from Feb 13, 2023
71205-849-72	71205084972	120 TABLET in 1 BOTTLE (71205-849-72)Marketed from Feb 13, 2023
71205-849-78	71205084978	180 TABLET in 1 BOTTLE (71205-849-78)Marketed from Feb 13, 2023
71205-849-90	71205084990	90 TABLET in 1 BOTTLE (71205-849-90)Marketed from Nov 1, 2020

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 — 64.8 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LP
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Nov 1, 2020
Listing expires: Dec 31, 2026
DEA schedule: CIV
Identifiers: Product ID 71205-849_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

N471205084900 followed by a unit qualifier and the quantity

Package 71205-0849-00. 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 Feb 1, 2023.

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.

Full label on DailyMed (opens in a new tab)