ACETAMINOPHEN AND CODEINE PHOSPHATE
- Product NDC
- 61919-273
- 11-digit product format
- 619190273
- Labeler code
- 61919
- Product ID
- 61919-273_2fe3ae02-4bb8-4ebf-bf12-d9e6828ba46b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ACETAMINOPHEN AND CODEINE PHOSPHATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA088629
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- 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
- 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 |
|---|
| 61919-273-90 | ACETAMINOPHEN AND CODEINE PHOSPHATE | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-273 | ACETAMINOPHEN AND CODEINE PHOSPHATE TABLET [DIRECTRX] | 1 | Legacy NDC, 1 package rows | 20151027_0d4a1024-85a2-4339-8c94-33f1a64d0b11.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-273-90 | 61919027390 | 90 in 1 BOTTLE | Historical |