Pain Relief PM
- Product NDC
- 76168-011
- 11-digit product format
- 761680011
- Labeler code
- 76168
- Product ID
- 76168-011_e0595668-bbee-4f87-92cb-2a987105d2c0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen PM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Velocity Pharma
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-12-05
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 500 mg/1; mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 76168-011-04 | Pain Relief PM | 24 in 1 BOTTLE | TABLET | 24 | | 1 |
| 76168-011-04 | Pain Relief PM | 1 in 1 CARTON | TABLET | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76168-011 | PAIN RELIEF PM (ACETAMINOPHEN PM) TABLET [VELOCITY PHARMA] | 1 | Legacy NDC, 2 package rows | 20130829_1a49129b-381d-4be4-baa1-c1ba5f00b312.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76168-011-04 | 76168001104 | 24 in 1 BOTTLE | Historical |