Acetaminophen and Codeine Phosphate
- Product NDC
- 82804-283
- 11-digit product format
- 828040283
- Labeler code
- 82804
- Product ID
- 82804-283_917e4926-1e60-473e-9ed8-b9abe08d83f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetaminophen and Codeine Phosphate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA212418
- Marketing category
- ANDA
- Marketing start
- 2019-09-10
- Substance
- ACETAMINOPHEN; CODEINE PHOSPHATE
- Active strength
- 300; 30 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Acetaminophen and Codeine Phosphate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 300 mg/1 |
| CODEINE PHOSPHATE | 30 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D, GSL05Y1MN6 |
| Rxcui | 993781 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82804-283-20 | Acetaminophen and Codeine Phosphate | 20 in 1 BOTTLE | TABLET | 20 | | 2 |
| 82804-283-30 | Acetaminophen and Codeine Phosphate | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-283-20 | 82804028320 | 20 TABLET in 1 BOTTLE (82804-283-20) | 20 tablet | 2026-05-14 | No | No | Current |
| 82804-283-30 | 82804028330 | 30 TABLET in 1 BOTTLE (82804-283-30) | 30 tablet | 2026-04-21 | No | No | Current |