BC
- Product NDC
- 63029-215
- 11-digit product format
- 630290215
- Labeler code
- 63029
- Product ID
- 63029-215_f7e5b2ad-68d8-45a6-8ee0-c8c29e590f57
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Medtech Products Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-05-07
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 650 mg/1; mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63029-215-04 | 63029021504 | 4 POWDER in 1 CARTON (63029-215-04) | 4 powder | 2018-05-07 | 0000-00-00 | No | No | Current |
| 63029-215-12 | 63029021512 | 12 POWDER in 1 CARTON (63029-215-12) | 12 powder | 2018-05-07 | 0000-00-00 | No | No | Current |