ACETAMINOPHEN AND CODEINE
- Product NDC
- 61919-472
- 11-digit product format
- 619190472
- Labeler code
- 61919
- Product ID
- 61919-472_54153740-88fd-49f9-857f-1ee544adb9ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ACETAMINOPHEN AND CODEINE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA089828
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- CODEINE PHOSPHATE; ACETAMINOPHEN
- Active strength
- 60 mg/1; mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-472-90 | ACETAMINOPHEN AND CODEINE | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-472 | ACETAMINOPHEN AND CODEINE TABLET [DIRECT RX] | 3 | Legacy NDC, 1 package rows | 20150602_3c4ccc93-1b1a-4daa-95f8-6ea2a2fc9811.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-472-90 | 61919047290 | 90 in 1 BOTTLE | Historical |