Maxichlor PEH DM
- Product NDC
- 58605-103
- 11-digit product format
- 586050103
- Labeler code
- 58605
- Product ID
- 58605-103_9f6e84e3-dba2-4c15-bdcf-bc2c0450f1d9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MCR American Pharmaceuticals, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-04-01
- Marketing end
- 0000-00-00
- Substance
- CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 4 mg/1; mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 58605-103-01 | Maxichlor PEH DM | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 1 |
| 58605-103-20 | Maxichlor PEH DM | 20 in 1 BLISTER PACK | TABLET | 20 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58605-103 | MAXICHLOR PEH DM (CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE) TABLET [MCR AMERICAN PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 2 package rows | 20180401_70bb5a77-8a9b-4794-93e7-90c21482fb8b.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 |
|---|
| 58605-103-01 | 58605010301 | 100 TABLET in 1 BOTTLE, PLASTIC (58605-103-01) | 100 tablet | 2018-04-01 | 0000-00-00 | No | No | Current |
| 58605-103-20 | 58605010320 | 20 TABLET in 1 BLISTER PACK (58605-103-20) | 20 tablet | 2018-04-01 | 0000-00-00 | No | No | Current |