ACETAMINOPHEN AND CODEINE PHOSPHATE
- Product NDC
- 63629-1186
- 11-digit product format
- 636291186
- Labeler code
- 63629
- Product ID
- 63629-1186_b110ac90-974f-4c7d-b315-274715e95c6c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acetaminophen and codeine phosphate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211610
- Marketing category
- ANDA
- Marketing start
- 2020-09-01
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; CODEINE PHOSPHATE
- Active strength
- 300 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CIII
- 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 |
|---|
| 63629-1186-1 | 63629118601 | 100 TABLET in 1 BOTTLE (63629-1186-1) | 100 tablet | 2020-09-01 | 0000-00-00 | No | No | Current |