Anatra
- Product NDC
- 83641-001
- 11-digit product format
- 836410001
- Labeler code
- 83641
- Product ID
- 83641-001_4097d2e5-5d3f-b62a-e063-6294a90a882f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Anas Barbariae
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Anatra LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2023-09-01
- Substance
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE
- Active strength
- 200 [hp_C]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Anatra
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE | 200 [hp_C]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | RN2HC612GY |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83641-001-01 | Anatra | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 3 |
| 83641-001-02 | Anatra | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83641-001 | ANATRA (ANAS BARBARIAE) TABLET [ANATRA LLC] | 2 | Current NDC, 2 package rows | 20250115_4562fa87-ed88-42fb-b530-e600aea351d9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83641-001-01 | 83641000101 | 30 TABLET in 1 BOTTLE, PLASTIC (83641-001-01) | 30 tablet | 2023-09-01 | No | No | Historical |
| 83641-001-02 | 83641000102 | 60 TABLET in 1 BOTTLE, PLASTIC (83641-001-02) | 60 tablet | 2023-09-01 | No | No | Historical |