Pseudoephedrine hydrochloride
- Product NDC
- 85766-050
- 11-digit product format
- 857660050
- Labeler code
- 85766
- Product ID
- 85766-050_4a2c19fc-1529-0713-e063-6394a90a87fe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pseudoephedrine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sportpharm LLC
- Application
- ANDA077442
- Marketing category
- ANDA
- Marketing start
- 2006-04-28
- Substance
- PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 120 mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pseudoephedrine hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PSEUDOEPHEDRINE HYDROCHLORIDE | 120 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6V9V2RYJ8N |
| Rxcui | 1049154 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85766-050-10 | Pseudoephedrine hydrochloride | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 85766-050-10 | 85766005010 | 10 TABLET, FILM COATED in 1 BLISTER PACK (85766-050-10) | 2025-08-02 | No | No | Historical |