EXTRA STRENGTH PAIN RELIEF
- Product NDC
- 61919-271
- 11-digit product format
- 619190271
- Labeler code
- 61919
- Product ID
- 61919-271_b855548f-ebc0-6dc8-e053-2995a90a6632
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-07-30
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-271-50 | 61919027150 | 50 TABLET in 1 BOTTLE (61919-271-50) | 50 tablet | 2018-03-14 | 0000-00-00 | No | No | Current |
| 61919-271-60 | 61919027160 | 60 TABLET in 1 BOTTLE (61919-271-60) | 60 tablet | 2019-07-30 | 0000-00-00 | No | No | Current |
| 61919-271-71 | 61919027171 | 100 TABLET in 1 BOTTLE (61919-271-71) | 100 tablet | 2019-07-30 | 0000-00-00 | No | No | Current |