Acetaminophen and Codeine Phosphate
- Product NDC
- 71205-001
- 11-digit product format
- 712050001
- Labeler code
- 71205
- Product ID
- 71205-001_a287ed41-2a8c-4181-9d55-9994aa9b0769
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acetaminophen and Codeine Phosphate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA088628
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-001 | ACETAMINOPHEN AND CODEINE PHOSPHATE TABLET [PROFICIENT RX LP] | 4 | Legacy NDC | 20191122_337b80a6-0398-43be-bd22-288332d9c4d0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-001-15 | 71205000115 | 15 TABLET in 1 BOTTLE (71205-001-15) | 15 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |
| 71205-001-20 | 71205000120 | 20 TABLET in 1 BOTTLE (71205-001-20) | 20 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |
| 71205-001-30 | 71205000130 | 30 TABLET in 1 BOTTLE (71205-001-30) | 30 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |
| 71205-001-60 | 71205000160 | 60 TABLET in 1 BOTTLE (71205-001-60) | 60 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |
| 71205-001-90 | 71205000190 | 90 TABLET in 1 BOTTLE (71205-001-90) | 90 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |