Maxiphen
- Product NDC
- 58605-422
- 11-digit product format
- 586050422
- Labeler code
- 58605
- Product ID
- 58605-422_688d38bc-8d53-4103-8041-9da8184b73b6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GUAIFENESIN and Phenylephrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MCR American Pharmaceuticals, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2008-03-31
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 400 mg/1; mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 58605-422-01 | 2020-05-20 | C162847 | 48780-1 | 97449f38-b78f-f6ea-e053-dbdaa90aa703 | 08233978-db81-48a9-a4e6-5b5b4f19e420 |
| 58605-422-02 | 2020-05-20 | C162847 | 48780-1 | 97449f38-b78f-f6ea-e053-dbdaa90aa703 | 08233978-db81-48a9-a4e6-5b5b4f19e420 |
| 58605-422-01 | 2019-11-13 | C162847 | 48780-1 | 97449f38-b78f-f6ea-e053-dbdaa90aa703 | 08233978-db81-48a9-a4e6-5b5b4f19e420 |
| 58605-422-02 | 2019-11-13 | C162847 | 48780-1 | 97449f38-b78f-f6ea-e053-dbdaa90aa703 | 08233978-db81-48a9-a4e6-5b5b4f19e420 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 58605-422-01 | EA - Each | 58605-422 | 79753d0c-44ed-4cb4-9568-1c1c7aaa9cea | 1 | 2013-02-13 |