BRYONIA ALBA
- Product NDC
- 60512-1007
- 11-digit product format
- 605121007
- Labeler code
- 60512
- Product ID
- 60512-1007_82538f88-1e66-4df2-8ddc-377a0759248a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BRYONIA ALBA
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- HOMEOLAB USA INC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1995-10-11
- Marketing end
- 0000-00-00
- Substance
- BRYONIA ALBA ROOT
- Active strength
- 3 [hp_X]/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60512-1007 | BRYONIA ALBA PELLET [HOMEOLAB USA INC] | 1 | Legacy NDC | 20111205_d2c9b2f0-4d04-4272-97e3-d8c6faa51089.zip |