Ibuprofen and Pseudoephedrine Hydrochloride
- Product NDC
- 37808-324
- 11-digit product format
- 378080324
- Labeler code
- 37808
- Product ID
- 37808-324_a5cf46a0-e3e5-4547-9360-352bd6d7d587
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen and Pseudoephedrine Hydrochloride
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- HEB
- Application
- ANDA074567
- Marketing category
- ANDA
- Marketing start
- 2018-04-17
- 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 |
|---|
| 37808-324-40 | 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 |
|---|
| 37808-324 | IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, SUGAR COATED [HEB] | 1 | Legacy NDC, 1 package rows | 20180712_af054e00-9171-4f73-8082-38b2b2eaba85.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 37808-324-40 | 37808032440 | 40 in 1 BLISTER PACK | Historical |