Butalbital, Acetaminophen, and Caffeine
- Product NDC
- 50436-1695
- 11-digit product format
- 504361695
- Labeler code
- 50436
- Product ID
- 50436-1695_2f9da74c-ea7d-43fd-bd08-5f2f8762b179
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Butalbital, Acetaminophen, and Caffeine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- 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]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50436-1695-1 | Butalbital, Acetaminophen, and Caffeine | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
| 50436-1695-2 | Butalbital, Acetaminophen, and Caffeine | 60 in 1 BOTTLE | TABLET | 60 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-1695 | BUTALBITAL, ACETAMINOPHEN, AND CAFFEINE TABLET [UNIT DOSE SERVICES] | 4 | Legacy NDC, 2 package rows | 20180523_b7e8a3c5-9da8-4609-9907-7de9e3243f7d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-1695-1 | 50436169501 | 30 in 1 BOTTLE | Historical |
| 50436-1695-2 | 50436169502 | 60 in 1 BOTTLE | Historical |