Allergy relief-D
- Product NDC
- 51660-940
- 11-digit product format
- 516600940
- Labeler code
- 51660
- Product ID
- 51660-940_767603f0-b735-4513-97d9-6c69a0bf70e3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Ohm Laboratories Inc.
- Application
- ANDA090922
- Marketing category
- ANDA
- Marketing start
- 2017-05-02
- Substance
- CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 5; 120 mg/1; mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Allergy relief-D
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CETIRIZINE HYDROCHLORIDE | 5 mg/1 |
| PSEUDOEPHEDRINE HYDROCHLORIDE | 120 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 64O047KTOA, 6V9V2RYJ8N |
| Rxcui | 1014571 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51660-940-12 | Allergy relief-D | 2 in 1 CARTON | TABLET, FILM COATED, EXTENDED RE | 2 | | 5 |
| 51660-940-12 | Allergy relief-D | 6 in 1 BLISTER PACK | TABLET, FILM COATED, EXTENDED RE | 6 | | 5 |
| 51660-940-24 | Allergy relief-D | 4 in 1 CARTON | TABLET, FILM COATED, EXTENDED RE | 4 | | 5 |
| 51660-940-24 | Allergy relief-D | 6 in 1 BLISTER PACK | TABLET, FILM COATED, EXTENDED RE | 6 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51660-940 | ALLERGY RELIEF-D (CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [OHM LABORATORIES INC.] | 5 | Current NDC, Legacy NDC, 4 package rows | 20250101_c24f3760-70e0-410f-bf80-6d0cadcd61b9.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 |
|---|
| 51660-940-12 | 51660094012 | 2 BLISTER PACK in 1 CARTON (51660-940-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2017-05-02 | 0000-00-00 | No | No | Current |
| 51660-940-24 | 51660094024 | 4 BLISTER PACK in 1 CARTON (51660-940-24) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | 4 blister pack | 2017-05-02 | 0000-00-00 | No | No | Current |