Acetaminophen
- Product NDC
- 11822-6304
- 11-digit product format
- 118226304
- Labeler code
- 11822
- Product ID
- 11822-6304_fe2733e1-fb59-4f5e-a5da-8897b3e352ad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA211544
- Marketing category
- ANDA
- Marketing start
- 2020-05-29
- Marketing end
- 2025-05-29
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-6304 | ACETAMINOPHEN EXTENDED RELEASE (ACETAMINOPHEN) TABLET [RITE AID CORPORATION] | 4 | Legacy NDC | 20221104_bb5fc500-c455-48e2-9a3e-a534b8216596.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-6304-1 | 11822630401 | 1 BOTTLE, PLASTIC in 1 BOX (11822-6304-1) > 50 TABLET in 1 BOTTLE, PLASTIC | | 2020-05-29 | 0000-00-00 | No | No | Current |
| 11822-6304-2 | 11822630402 | 1 BOTTLE, PLASTIC in 1 BOX (11822-6304-2) > 100 TABLET in 1 BOTTLE, PLASTIC | | 2020-05-29 | 0000-00-00 | No | No | Current |
| 11822-6304-3 | 11822630403 | 225 TABLET in 1 BOTTLE, PLASTIC (11822-6304-3) | 225 tablet | 2020-05-29 | 0000-00-00 | No | No | Current |