NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2546Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2546Add 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
71335-2546-0713352546007133525460084 TABLET in 1 BOTTLE, PLASTIC (71335-2546-0)Marketed from Jan 17, 2025
71335-2546-1713352546017133525460120 TABLET in 1 BOTTLE, PLASTIC (71335-2546-1)Marketed from Jan 17, 2025
71335-2546-2713352546027133525460230 TABLET in 1 BOTTLE, PLASTIC (71335-2546-2)Marketed from Jan 17, 2025
71335-2546-3713352546037133525460360 TABLET in 1 BOTTLE, PLASTIC (71335-2546-3)Marketed from Jan 17, 2025
71335-2546-4713352546047133525460490 TABLET in 1 BOTTLE, PLASTIC (71335-2546-4)Marketed from Jan 17, 2025
71335-2546-5713352546057133525460550 TABLET in 1 BOTTLE, PLASTIC (71335-2546-5)Marketed from Jan 17, 2025
71335-2546-671335254606713352546066 TABLET in 1 BOTTLE, PLASTIC (71335-2546-6)Marketed from Jan 17, 2025
71335-2546-77133525460771335254607120 TABLET in 1 BOTTLE, PLASTIC (71335-2546-7)Marketed from Jan 17, 2025
71335-2546-8713352546087133525460840 TABLET in 1 BOTTLE, PLASTIC (71335-2546-8)Marketed from Jan 17, 2025
71335-2546-9713352546097133525460912 TABLET in 1 BOTTLE, PLASTIC (71335-2546-9)Marketed from Jan 17, 2025

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

Generic name (nonproprietary)
butalbital, acetaminophen and caffeine
Active ingredients
Butalbital — 50 mg/1Acetaminophen — 325 mg/1Caffeine — 40 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
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 71335-2546_79ce2e93-19de-49dc-b30d-696ec421b030SPL ID 79ce2e93-19de-49dc-b30d-696ec421b030SPL set ID b9df47cf-f999-49d8-95b9-374c0539b6a1RxCUI 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

N471335254600 followed by a unit qualifier and the quantity

Package 71335-2546-00. 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 . 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)

About NDC 71335-2546

What is NDC 71335-2546?
71335-2546 is the product NDC for Butalbital, Acetaminophen And Caffeine, Butalbital 50 mg/1 + 2 more ingredients tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Butalbital, Acetaminophen And Caffeine.
What is the active ingredient?
Butalbital, Acetaminophen, Caffeine.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Butalbital, Acetaminophen And Caffeine?
50 other product NDCs are listed under this name. See all Butalbital, Acetaminophen And Caffeine NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Butalbital, Acetaminophen And Caffeine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Butalbital, Acetaminophen and CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralPreferred Pharmaceuticals Inc.68788-412668788-4126-0268788-4126-03
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralREMEDYREPACK INC.70518-460170518-4601-0070518-4601-0170518-4601-02
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsCapsuleOralAmici Pharma, Inc.69292-30569292-0305-01
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralAdvanced Rx of Tennessee, LLC80425-056780425-0567-0180425-0567-0280425-0567-03
Butalbital, Acetaminophen and Caffeinebutalbital, acetaminophen, and caffeineButalbital 50 mg/15mL + 2 more ingredientsSolutionOralGenus Lifesciences Inc.64950-29064950-0290-16
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsCapsuleOralAdvanced Rx of Tennessee, LLC80425-049780425-0497-01
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralPreferred Pharmaceuticals Inc.68788-879468788-8794-0268788-8794-03
butalbital, acetaminophen and caffeineButalbital 50 mg/1 + 2 more ingredientsCapsuleOralDr. Reddy's Labratories Inc.75907-00975907-0009-01
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralQUAGEN PHARMACEUTICALS LLC70752-14270752-0142-1070752-0142-14
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsCapsuleOralQUAGEN PHARMACEUTICALS LLC70752-14470752-0144-1070752-0144-14

All 51 Butalbital, Acetaminophen And Caffeine NDCs

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 ingredientsTabletOralPreferred Pharmaceuticals Inc.68788-8794
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralBryant Ranch Prepack72162-2666
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralQUAGEN PHARMACEUTICALS LLC70752-142
Butalbital, Acetaminophen And CaffeineButalbital 50 mg/1 + 2 more ingredientsTabletOralBryant Ranch Prepack71335-2630
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

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