Bovista 200C
- Product NDC
- 69152-1052
- 11-digit product format
- 691521052
- Labeler code
- 69152
- Product ID
- 69152-1052_2f588b95-5964-63dd-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bovista
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Paramesh Banerji Life Sciences LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-06-15
- Marketing end
- 0000-00-00
- Substance
- LYCOPERDON UTRIFORME FRUITING BODY
- Active strength
- 200 [hp_C]/1
- 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 |
|---|
| 69152-1052-1 | Bovista 200C | 96 in 1 BOTTLE | PELLET | 96 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69152-1052 | BOVISTA 200C (BOVISTA) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC] | 2 | Legacy NDC, 1 package rows | 20160331_1888f734-c35d-3bf4-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69152-1052-1 | 69152105201 | 96 in 1 BOTTLE | Historical |