PlusPharma Extra Strength
- Product NDC
- 51645-706
- 11-digit product format
- 516450706
- Labeler code
- 51645
- Product ID
- 51645-706_e8f7bed1-18ee-b041-e053-2a95a90a087f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Gemini Pharmaceuticals, Inc. dba Plus Pharma
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2006-03-27
- Marketing end
- 2023-12-31
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51645-706-01 | 51645070601 | 100 TABLET in 1 BOTTLE, PLASTIC (51645-706-01) | 100 tablet | 2006-03-27 | 0000-00-00 | No | No | Current |
| 51645-706-10 | 51645070610 | 1000 TABLET in 1 BOTTLE, PLASTIC (51645-706-10) | 1000 tablet | 2006-03-27 | 0000-00-00 | No | No | Current |