Baptisia tinctoria
- Product NDC
- 63083-7105
- 11-digit product format
- 630837105
- Labeler code
- 63083
- Product ID
- 63083-7105_6138981c-237e-4073-8467-d9525e9af855
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Baptisia tinctoria
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Marketing end
- 0000-00-00
- Substance
- BAPTISIA TINCTORIA WHOLE
- Active strength
- 6 [hp_X]/29.5mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63083-7105 | BAPTISIA TINCTORIA 7105 (BAPTISIA TINCTORIA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Legacy NDC | 20220218_6d06eb17-32c6-4ca7-b05b-5fc2e7a086cc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-7105-1 | 63083710501 | 29.5 mL in 1 BOTTLE, DROPPER (63083-7105-1) | 29.5 ml | 1985-08-15 | 0000-00-00 | No | No | Current |