Childrens Acetaminophen
- Product NDC
- 0121-0939
- 11-digit product format
- 001210939
- Labeler code
- 0121
- Product ID
- 0121-0939_e5d6567e-a8f6-5bb7-e053-2a95a90a0f87
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Pharmaceutical Associates, Inc.
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-01-29
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0121-0939-00 | 00121093900 | 10 TRAY in 1 CASE (0121-0939-00) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (0121-0939-05) | 10 tray | 2021-02-05 | 0000-00-00 | No | No | Current |