ALLERGY RELIEF
- Product NDC
- 73581-203
- 11-digit product format
- 735810203
- Labeler code
- 73581
- Product ID
- 73581-203_0e1383b5-910b-fabb-e063-6394a90a0a30
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LORATADINE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- YYBA CORP
- Application
- ANDA208314
- Marketing category
- ANDA
- Marketing start
- 2021-07-28
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- 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
- Brand name suffix
- 10mg
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LORATADINE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7AJO3BO7QN |
| Rxcui | 311372 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73581-203-01 | ALLERGY RELIEF10mg | 100 in 1 BOTTLE | TABLET | 100 | | 7 |
| 73581-203-36 | ALLERGY RELIEF10mg | 365 in 1 BOTTLE | TABLET | 365 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73581-203 | ALLERGY RELIEF 10MG (LORATADINE) TABLET [YYBA CORP] | 7 | Current NDC, Legacy NDC, 2 package rows | 20240104_6103cf98-40b1-4d27-8eb7-6f6a06949730.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 |
|---|
| 73581-203-01 | 73581020301 | 100 TABLET in 1 BOTTLE (73581-203-01) | 100 tablet | 2021-07-28 | 0000-00-00 | No | No | Current |
| 73581-203-36 | 73581020336 | 365 TABLET in 1 BOTTLE (73581-203-36) | 365 tablet | 2021-07-28 | 0000-00-00 | No | No | Current |