Butalbital, Acetaminophen, and Caffeine
- Product NDC
- 50090-2564
- 11-digit product format
- 500902564
- Labeler code
- 50090
- Product ID
- 50090-2564_93bdf8ab-5432-4514-9807-5125c54219a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Butalbital, Acetaminophen, and Caffeine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA200243
- Marketing category
- ANDA
- Marketing start
- 2012-09-13
- Marketing end
- 0000-00-00
- Substance
- BUTALBITAL; ACETAMINOPHEN; CAFFEINE
- Active strength
- 50 mg/1; mg/1; mg/1
- Pharmacologic classes
- Barbiturates [CS],Barbiturate [EPC],Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2564-0 | Butalbital, Acetaminophen, and Caffeine | 30 in 1 BOTTLE | TABLET | 30 | | 8 |
| 50090-2564-3 | Butalbital, Acetaminophen, and Caffeine | 100 in 1 BOTTLE | TABLET | 100 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2564 | BUTALBITAL, ACETAMINOPHEN, AND CAFFEINE TABLET [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC, 2 package rows | 20190225_63e4e76a-7422-4c46-8aca-dc1a5d50f45a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2564-0 | 50090256400 | 30 in 1 BOTTLE | Historical |
| 50090-2564-3 | 50090256403 | 100 in 1 BOTTLE | Historical |