Tussin Expectorant
- Product NDC
- 76281-507
- 11-digit product format
- 762810507
- Labeler code
- 76281
- Product ID
- 76281-507_46e2f5c3-5d72-c4d3-e063-6294a90a74a0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GUAIFENESIN
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- AptaPharma, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-09-30
- Substance
- GUAIFENESIN
- Active strength
- 100 mg/5mL
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tussin Expectorant
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GUAIFENESIN | 100 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 310604 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76281-507-24 | Tussin Expectorant | 118 mL in 1 BOTTLE | LIQUID | 118 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76281-507 | TUSSIN EXPECTORANT (GUAIFENESIN) LIQUID [APTAPHARMA, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20231231_ca8fa216-09c1-42b2-a95b-fa3d0f13363c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76281-507-24 | 76281050724 | 118 mL in 1 BOTTLE (76281-507-24) | 118 ml | 2020-09-30 | 0000-00-00 | No | No | Current |