BiPla
- Product NDC
- 52964-1001
- 11-digit product format
- 529641001
- Labeler code
- 52964
- Product ID
- 52964-1001_4f9da83d-75f7-47c1-8bfc-9d78267c9e9a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SUS SCROFA PLACENTA
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- TMN K.K.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-08-02
- Marketing end
- 0000-00-00
- Substance
- SUS SCROFA PLACENTA
- Active strength
- 16000 mg/30mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52964-1001-1 | BiPla | 30 mL in 1 BOTTLE, GLASS | LIQUID | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52964-1001 | BIPLA (SUS SCROFA PLACENTA) LIQUID [TMN K.K.] | 1 | Legacy NDC, 1 package rows | 20120812_91f9b962-ffb4-4cf1-9154-116d24cbeff1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 52964-1001-1 | 52964100101 | 30 mL in 1 BOTTLE, GLASS | 30 ml | Historical |