Mucus Relief Extended Release
- Product NDC
- 69256-732
- 11-digit product format
- 692560732
- Labeler code
- 69256
- Product ID
- 69256-732_a12aed31-c80c-440b-a805-980f56bee705
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Harris Teeter, LLC
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2021-05-28
- Marketing end
- 2026-05-28
- Substance
- GUAIFENESIN
- Active strength
- 1200 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Current FDA listing
- Yes
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69256-732 | MUCUS RELIEF EXTENDED RELEASE MAXIMUM STRENGTH (GUAIFENESIN) TABLET [HARRIS TEETER, LLC] | 3 | Current NDC, Legacy NDC | 20250306_e1ca82fe-224f-4cdd-9992-2754c1e508e1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69256-732-14 | 69256073214 | 14 BLISTER PACK in 1 CARTON (69256-732-14) / 1 TABLET in 1 BLISTER PACK | 14 blister pack | 2021-05-28 | 2026-05-28 | No | No | Current |