NDC codes

FDA NDC Directory
Product NDC (as listed)70752-142Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70752-0142Add 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
70752-142-1070752014210100 TABLET in 1 BOTTLE, PLASTIC (70752-142-10)Marketed from May 1, 2024
70752-142-1470752014214500 TABLET in 1 BOTTLE, PLASTIC (70752-142-14)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, 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 214287
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 70752-142_33f4fcf9-9767-4d27-bae3-9c0698f568e1SPL ID 33f4fcf9-9767-4d27-bae3-9c0698f568e1SPL set ID 24813ec6-0111-4782-9182-a2b93501a2bcRxCUI 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

N470752014210 followed by a unit qualifier and the quantity

Package 70752-0142-10. 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, acetaminophen and caffeine 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)

Other NDCs under ANDA 214287

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

FDA NDC Directory listings under ANDA 214287
ProductStrengthForm · routeLabelerProduct NDC
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralBryant Ranch Prepack71335-2630
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralPreferred Pharmaceuticals Inc.68788-8794
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralAdvanced Rx of Tennessee, LLC80425-0567
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralREMEDYREPACK INC.70518-4601
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralBryant Ranch Prepack71335-2546
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralBryant Ranch Prepack72162-2666

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