Acetaminophen
- Product NDC
- 15127-332
- 11-digit product format
- 151270332
- Labeler code
- 15127
- Product ID
- 15127-332_52cde4d1-9930-4d53-9c28-2dcc281867d2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Select Brand
- Application
- ANDA076200
- Marketing category
- ANDA
- Marketing start
- 2002-04-30
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 15127-332-01 | Acetaminophen | 100 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 100 | | 1 |
| 15127-332-24 | Acetaminophen | 24 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 24 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| ACETAMINOPHEN | ACTIVE INGREDIENT | 362O9ITL9D | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| ACETAMINOPHEN | ACTIVE MOIETY | 362O9ITL9D | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| PROPYLENE GLYCOL | INACTIVE INGREDIENT | 6DC9Q167V3 | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| STARCH, PREGELATINIZED CORN | INACTIVE INGREDIENT | O8232NY3SJ | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 15127-332 | ACETAMINOPHEN TABLET, FILM COATED, EXTENDED RELEASE [SELECT BRAND] | 1 | Legacy NDC, 2 package rows | 20130214_80310ab1-f10f-4881-b31a-fa156db8e474.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 15127-332-01 | 15127033201 | 100 in 1 BOTTLE | Historical |
| 15127-332-24 | 15127033224 | 24 in 1 BOTTLE | Historical |