Maxi-Tuss AC
- Product NDC
- 58605-313
- 11-digit product format
- 586050313
- Labeler code
- 58605
- Product ID
- 58605-313_829932e9-5ecb-4b19-8807-725a69d69339
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CODEINE PHOSPHATE and GUAIFENESIN
- Dosage form
- LIQUID
- 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
- CODEINE PHOSPHATE; GUAIFENESIN
- Active strength
- 10 mg/5mL; mg/5mL
- DEA schedule
- CV
- 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 |
|---|
| 58605-313-16 | Maxi-Tuss AC | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58605-313 | MAXI-TUSS AC (CODEINE PHOSPHATE AND GUAIFENESIN) LIQUID [MCR AMERICAN PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 1 package rows | 20200801_4df08753-dc51-41f4-a8a7-11a76b318b02.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 |
|---|
| 58605-313-16 | 58605031316 | 473 mL in 1 BOTTLE, PLASTIC (58605-313-16) | 473 ml | 2020-08-01 | 0000-00-00 | No | No | Current |