Maxi-Tuss CD
- Product NDC
- 58605-303
- 11-digit product format
- 586050303
- Labeler code
- 58605
- Product ID
- 58605-303_9daf272d-ba0b-4f84-892b-0dc6e6f1abbd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CHLORPHENIRAMINE MALEATE, CODEINE PHOSPHATE, and PHENYLEPHRINE HYDROCHLORIDE
- Dosage form
- LIQUID
- 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; CODEINE PHOSPHATE; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 4 mg/5mL; mg/5mL; mg/5mL
- DEA schedule
- CV
- 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 |
|---|
| 58605-303-10 | Maxi-Tuss CD | 10 mL in 1 BOTTLE, PLASTIC | LIQUID | 10 | | 4 |
| 58605-303-16 | Maxi-Tuss CD | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58605-303 | MAXI-TUSS CD (CHLORPHENIRAMINE MALEATE, CODEINE PHOSPHATE, AND PHENYLEPHRINE HYDROCHLORIDE) LIQUID [MCR AMERICAN PHARMACEUTICALS, INC.] | 4 | Legacy NDC, 2 package rows | 20190822_e03294a3-1b3e-4d24-ac35-eca00a19db3d.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 |
|---|
| 58605-303-10 | 58605030310 | 10 mL in 1 BOTTLE, PLASTIC (58605-303-10) | 10 ml | 2018-04-01 | 0000-00-00 | No | No | Current |
| 58605-303-16 | 58605030316 | 473 mL in 1 BOTTLE, PLASTIC (58605-303-16) | 473 ml | 2018-04-01 | 0000-00-00 | No | No | Current |