Maxifed TR
- Product NDC
- 58605-106
- 11-digit product format
- 586050106
- Labeler code
- 58605
- Product ID
- 58605-106_f75d1e41-3e3a-440a-9768-4bfb71d7668d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- pseudoephedrine hydrochloride and triprolidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MCR American Pharmaceuticals, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-08-01
- Marketing end
- 0000-00-00
- Substance
- PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
- Active strength
- 30 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 58605-106-01 | Maxifed TR | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58605-106 | MAXIFED TR (PSEUDOEPHEDRINE HYDROCHLORIDE AND TRIPROLIDINE HYDROCHLORIDE) TABLET [MCR AMERICAN PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 1 package rows | 20200801_daf47021-cf49-4d6f-9dbf-2d0a69da4c9c.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 |
|---|
| 58605-106-01 | 58605010601 | 100 TABLET in 1 BOTTLE, PLASTIC (58605-106-01) | 100 tablet | 2020-08-01 | 0000-00-00 | No | No | Current |