Anacardium Occidentale
- Product NDC
- 63545-970
- 11-digit product format
- 635450970
- Labeler code
- 63545
- Product ID
- 63545-970_2b4ac32a-66dd-9a05-e063-6294a90a1016
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Anacardium Occidentale
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Hahnemann Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-11-02
- Substance
- ANACARDIUM OCCIDENTALE FRUIT
- Active strength
- 1 [hp_Q]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Anacardium Occidentale
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ANACARDIUM OCCIDENTALE FRUIT | 1 [hp_Q]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4A10JR4E7E |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63545-970-01 | Anacardium Occidentale | 10000 in 1 BOTTLE, GLASS | PELLET | 10000 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63545-970 | ANACARDIUM OCCIDENTALE PELLET [HAHNEMANN LABORATORIES, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250112_b325974f-206e-5fa1-e053-2995a90aa1dd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63545-970-01 | 63545097001 | 10000 PELLET in 1 BOTTLE, GLASS (63545-970-01) | 10000 pellet | 2020-11-02 | 0000-00-00 | No | No | Current |