Ibuprofen and Pseudoephedrine Hydrochloride
- Product NDC
- 53943-423
- 11-digit product format
- 539430423
- Labeler code
- 53943
- Product ID
- 53943-423_1cfcd39c-e0fe-45d8-be1b-9064d62613c4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen and Pseudoephedrine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- Discount Drug Mart
- Application
- ANDA074567
- Marketing category
- ANDA
- Marketing start
- 2001-10-13
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 200 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53943-423-21 | Ibuprofen and Pseudoephedrine Hydrochloride | 40 in 1 BLISTER PACK | TABLET, SUGAR COATED | 40 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53943-423 | IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, SUGAR COATED [DISCOUNT DRUG MART] | 1 | Legacy NDC, 1 package rows | 20180525_815be4dc-2924-4912-833a-3e8ebd2f8f2b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53943-423-21 | 53943042321 | 40 in 1 BLISTER PACK | Historical |