ALLOXANUM
- Product NDC
- 60512-6161
- 11-digit product format
- 605126161
- Labeler code
- 60512
- Product ID
- 60512-6161_e030028c-1409-4ff7-a96d-f5b4ae8f4000
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALLOXANUM
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- HOMEOLAB USA INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1995-10-11
- Marketing end
- 0000-00-00
- Substance
- ALLOXAN
- Active strength
- 6 [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60512-6161 | ALLOXANUM PELLET [HOMEOLAB USA INC.] | 1 | Legacy NDC | 20131028_d3d02f8c-353a-43f5-952f-ad5ece830432.zip |