NDC codes

FDA NDC Directory
Product NDC (as listed)70752-148Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70752-0148Add 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 NDC11-digit (billing)PackageCopy
70752-148-1070752014810100 TABLET in 1 BOTTLE (70752-148-10)Marketed from May 1, 2024
70752-148-1470752014814500 TABLET in 1 BOTTLE (70752-148-14)Marketed from May 1, 2024

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)
BUTALBITAL and ACETAMINOPHEN
Generic name (nonproprietary)
butalbital and acetaminophen
Active ingredients
Butalbital50 mg/1Acetaminophen325 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214291
Marketing start
Listing expires
DEA schedule
CIII
Other FDA classes
Barbiturates (Chemical structure)
Identifiers
Product ID 70752-148_d113b27d-2b74-45ad-b095-d0cded8d4f6bSPL ID d113b27d-2b74-45ad-b095-d0cded8d4f6bSPL set ID 2eb09253-7f59-401e-afbc-70bb9600fedfRxCUI 197426UNII KHS0AZ4JVK, 362O9ITL9D
Pharmacologic class
Barbiturate

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

N470752014810 followed by a unit qualifier and the quantity

Package 70752-0148-10. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Butalbital and acetaminophen tablets are indicated for the relief of the symptom complex of tension (or muscle contraction) headache. Evidence supporting the efficacy and safety of this combination product in the treatment of multiple recurrent headaches is unavailable. Caution in this regard is required because butalbital is habit-forming and potentially abusable.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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