Allfen DM
- Product NDC
- 58605-401
- 11-digit product format
- 586050401
- Labeler code
- 58605
- Product ID
- 58605-401_f8c0fb86-2639-485f-9eaf-769dc32e49ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GUAIFENESIN and Dextromethorphan Hydrobromide
- 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; DEXTROMETHORPHAN HYDROBROMIDE
- 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 |
|---|---|---|---|---|---|
| 58605-401-01 | 2020-05-20 | C162847 | 48780-1 | 97449f38-c8db-f6ea-e053-dbdaa90aa703 | 17e44510-a6d3-479c-9ebc-20302dcb04cd |
| 58605-401-02 | 2020-05-20 | C162847 | 48780-1 | 97449f38-c8db-f6ea-e053-dbdaa90aa703 | 17e44510-a6d3-479c-9ebc-20302dcb04cd |
| 58605-401-01 | 2019-11-13 | C162847 | 48780-1 | 97449f38-c8db-f6ea-e053-dbdaa90aa703 | 17e44510-a6d3-479c-9ebc-20302dcb04cd |
| 58605-401-02 | 2019-11-13 | C162847 | 48780-1 | 97449f38-c8db-f6ea-e053-dbdaa90aa703 | 17e44510-a6d3-479c-9ebc-20302dcb04cd |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 58605-401-01 | EA - Each | 58605-401 | 4c050995-af02-4826-9e3e-4b0d4399419b | 1 | 2012-07-24 |