BUTALBITAL, ACETAMINOPHEN AND CAFFEINE
NDC 71335-2546, BUTALBITAL, ACETAMINOPHEN AND CAFFEINE, tablet, from Bryant Ranch Prepack.
- Product NDC
- 71335-2546
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214287
- DEA schedule
- CIII
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2546 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUTALBITAL50 mg/1
- ACETAMINOPHEN325 mg/1
- CAFFEINE40 mg/1
Pharmacologic classes
Barbiturate [EPC]; Barbiturates [CS]; Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]; Methylxanthine [EPC]; Xanthines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-2546-0 | 71335254600 | 84 TABLET in 1 BOTTLE, PLASTIC (71335-2546-0) |
| 71335-2546-1 | 71335254601 | 20 TABLET in 1 BOTTLE, PLASTIC (71335-2546-1) |
| 71335-2546-2 | 71335254602 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-2546-2) |
| 71335-2546-3 | 71335254603 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-2546-3) |
| 71335-2546-4 | 71335254604 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2546-4) |
| 71335-2546-5 | 71335254605 | 50 TABLET in 1 BOTTLE, PLASTIC (71335-2546-5) |
| 71335-2546-6 | 71335254606 | 6 TABLET in 1 BOTTLE, PLASTIC (71335-2546-6) |
| 71335-2546-7 | 71335254607 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-2546-7) |
| 71335-2546-8 | 71335254608 | 40 TABLET in 1 BOTTLE, PLASTIC (71335-2546-8) |
| 71335-2546-9 | 71335254609 | 12 TABLET in 1 BOTTLE, PLASTIC (71335-2546-9) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/b9df47cf-f999-49d8-95b9-374c0539b6a1
Use it
Look up 71335-2546 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2546 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2546. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.