Borrelia burgdorferi
- Product NDC
- 55714-6083
- 11-digit product format
- 557146083
- Labeler code
- 55714
- Product ID
- 55714-6083_b60c85d7-5ea4-aab9-e053-2a95a90a4361
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Borrelia burgdorferi
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Newton Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-08-01
- Marketing end
- 0000-00-00
- Substance
- BORRELIA BURGDORFERI
- Active strength
- 200 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55714-6083-1 | 55714608301 | 30 mL in 1 BOTTLE, GLASS (55714-6083-1) | 30 ml | 2011-08-01 | 0000-00-00 | No | No | Current |