Acetaminophen
- Product NDC
- 0781-9274
- 11-digit product format
- 007819274
- Labeler code
- 0781
- Product ID
- 0781-9274_2884e523-5f12-48d6-98dc-3a80cde524f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acetaminophen
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA204052
- Marketing category
- ANDA
- Marketing start
- 2020-12-06
- Substance
- ACETAMINOPHEN
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Acetaminophen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 483017 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0781-9274-06 | Acetaminophen | 100 mL in 1 VIAL, GLASS | INJECTION, SOLUTION | 100 | | 1 |
| 0781-9274-95 | Acetaminophen | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0781-9274 | ACETAMINOPHEN INJECTION, SOLUTION [SANDOZ INC] | 1 | Current NDC, Legacy NDC, 2 package rows | 20210824_2884e523-5f12-48d6-98dc-3a80cde524f8.zip |
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 |
|---|
| 0781-9274-06 | 00781927406 | 100 mL in 1 VIAL, GLASS | 100 ml | | | | | Historical |
| 0781-9274-95 | 00781927495 | 10 VIAL, GLASS in 1 CARTON (0781-9274-95) / 100 mL in 1 VIAL, GLASS (0781-9274-06) | | 2021-09-20 | 0000-00-00 | No | No | Current |