Butalbital and Acetaminophen
- Product NDC
- 73159-003
- 11-digit product format
- 731590003
- Labeler code
- 73159
- Product ID
- 73159-003_edaea35f-8879-77b2-e053-2995a90a722a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- butalbital and acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lacer Pharma, LLC
- Application
- ANDA203484
- Marketing category
- ANDA
- Marketing start
- 2015-12-04
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; BUTALBITAL
- Active strength
- 325 mg/1; mg/1
- Pharmacologic classes
- Barbiturate [EPC], Barbiturates [CS]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 73159-003-01 | 73159000301 | 100 TABLET in 1 BOTTLE (73159-003-01) | 100 tablet | 2022-11-17 | 0000-00-00 | No | No | Current |