NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2272Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2272Add 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
71335-2272-07133522720084 TABLET in 1 BOTTLE (71335-2272-0)Marketed from Nov 30, 2023
71335-2272-17133522720120 TABLET in 1 BOTTLE (71335-2272-1)Marketed from Nov 30, 2023
71335-2272-27133522720230 TABLET in 1 BOTTLE (71335-2272-2)Marketed from Nov 30, 2023
71335-2272-37133522720360 TABLET in 1 BOTTLE (71335-2272-3)Marketed from Nov 30, 2023
71335-2272-47133522720490 TABLET in 1 BOTTLE (71335-2272-4)Marketed from Nov 30, 2023
71335-2272-57133522720550 TABLET in 1 BOTTLE (71335-2272-5)Marketed from Nov 30, 2023
71335-2272-6713352272066 TABLET in 1 BOTTLE (71335-2272-6)Marketed from Nov 30, 2023
71335-2272-771335227207120 TABLET in 1 BOTTLE (71335-2272-7)Marketed from Nov 30, 2023
71335-2272-87133522720840 TABLET in 1 BOTTLE (71335-2272-8)Marketed from Nov 30, 2023
71335-2272-97133522720912 TABLET in 1 BOTTLE (71335-2272-9)Marketed from Nov 30, 2023

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)
Butalbital, Acetaminophen and Caffeine
Generic name (nonproprietary)
butalbital, acetaminophen and caffeine
Active ingredients
Butalbital — 50 mg/1Acetaminophen — 325 mg/1Caffeine — 40 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040864
Marketing start
Listing expires
DEA schedule
CIII
Other FDA classes
Barbiturates (Chemical structure)Central Nervous System Stimulation (Physiologic effect)Xanthines (Chemical structure)
Identifiers
Product ID 71335-2272_c421e413-0101-4319-9d31-93a666c56692SPL ID c421e413-0101-4319-9d31-93a666c56692SPL set ID 6e28cc29-a85a-44d0-9c5b-bd0934ece64dRxCUI 238154UNII KHS0AZ4JVK, 362O9ITL9D, 3G6A5W338E
Pharmacologic class
Barbiturate; Central Nervous System Stimulant; Methylxanthine

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

N471335227200 followed by a unit qualifier and the quantity

Package 71335-2272-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 040864

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 040864
ProductStrengthForm · routeLabelerProduct NDC
Butalbital, Acetaminophen and CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralGolden State Medical Supply, Inc.51407-556
Butalbital, Acetaminophen and CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralGranules Pharmaceuticals Inc.70010-149
Butalbital, Acetaminophen and CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralST. MARY'S MEDICAL PARK PHARMACY60760-865
Butalbital, Acetaminophen and CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralBryant Ranch Prepack71335-2270

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