butalbital and acetaminophen
- Product NDC
- 46672-856
- 11-digit product format
- 466720856
- Labeler code
- 46672
- Product ID
- 46672-856_9c6f46ea-3625-20fb-e053-2a95a90a603d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- butalbital and acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mikart, LLC
- Application
- ANDA207386
- Marketing category
- ANDA
- Marketing start
- 2016-11-15
- Marketing end
- 0000-00-00
- Substance
- BUTALBITAL; ACETAMINOPHEN
- Active strength
- 50 mg/1; mg/1
- Pharmacologic classes
- Barbiturates [CS],Barbiturate [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 46672-856-10 | 46672085610 | 100 TABLET in 1 BOTTLE (46672-856-10) | 100 tablet | 2016-11-15 | 0000-00-00 | No | No | Current |
| 46672-856-22 | 46672085622 | 2 TABLET in 1 BOTTLE (46672-856-22) | 2 tablet | 2016-11-15 | 0000-00-00 | No | No | Current |
| 46672-856-50 | 46672085650 | 500 TABLET in 1 BOTTLE (46672-856-50) | 500 tablet | 2016-11-15 | 0000-00-00 | No | No | Current |