Acetamiophen
- Product NDC
- 23155-202
- 11-digit product format
- 231550202
- Labeler code
- 23155
- Product ID
- 23155-202_6f876e7f-7ff9-4b09-b5ef-b1a8a00975ad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA207035
- Marketing category
- ANDA
- Marketing start
- 2018-06-01
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 23155-202-01 | 23155020201 | 1 BOTTLE in 1 CARTON (23155-202-01) > 100 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2018-06-01 | 0000-00-00 | No | No | Current |
| 23155-202-18 | 23155020218 | 20000 TABLET, EXTENDED RELEASE in 1 CONTAINER (23155-202-18) | | 2018-06-01 | 0000-00-00 | No | No | Current |
| 23155-202-64 | 23155020264 | 1 BOTTLE in 1 CARTON (23155-202-64) > 24 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2018-06-01 | 0000-00-00 | No | No | Current |
| 23155-202-65 | 23155020265 | 1 BOTTLE in 1 CARTON (23155-202-65) > 750 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2018-06-01 | 0000-00-00 | No | No | Current |