Harris Teeter Mucus Relief D
- Product NDC
- 69256-144
- 11-digit product format
- 692560144
- Labeler code
- 69256
- Product ID
- 69256-144_85cad90e-ecb9-4c87-b971-bf60578a5c2e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, pseudoephedrine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Harris Teeter, LLC
- Application
- ANDA091071
- Marketing category
- ANDA
- Marketing start
- 2016-09-16
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 600 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 69256-144 | HARRIS TEETER MUCUS RELIEF D (GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE) TABLET, EXTENDED RELEASE [HARRIS TEETER, LLC] | 2 | Legacy NDC | 20191213_fd920c9b-3c47-4f31-b9bb-7baf79cc3205.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69256-144-89 | 69256014489 | 18 BLISTER PACK in 1 CARTON (69256-144-89) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 18 blister pack | 2016-09-16 | 0000-00-00 | No | No | Current |