ACETAMINOPHEN AND CODEINE PHOSPHATE
- Product NDC
- 55154-7553
- 11-digit product format
- 551547553
- Labeler code
- 55154
- Product ID
- 55154-7553_a1a42c0e-791d-4e4e-900c-cc36764ecc9c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acetaminophen and codeine phosphate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA040419
- Marketing category
- ANDA
- Marketing start
- 2009-06-29
- 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
- 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 |
|---|
| 55154-7553-0 | 55154755300 | 10 BLISTER PACK in 1 BAG (55154-7553-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2009-06-29 | 0000-00-00 | No | No | Current |