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BiPla
BiPla - 52964-1001-1 - (SUS SCROFA PLACENTA)
Drug Information of BiPla
| Product NDC: | 52964-1001 |
| Proprietary Name: | BiPla |
| Non Proprietary Name: | SUS SCROFA PLACENTA |
| Active Ingredient(s): | 16000 mg/30mL & nbsp; SUS SCROFA PLACENTA |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BiPla
| Product NDC: | 52964-1001 |
| Labeler Name: | TMN K.K. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120802 |
Package Information of BiPla
| Package NDC: | 52964-1001-1 |
| Package Description: | 30 mL in 1 BOTTLE, GLASS (52964-1001-1) |
NDC Information of BiPla
| NDC Code | 52964-1001-1 |
| Proprietary Name | BiPla |
| Package Description | 30 mL in 1 BOTTLE, GLASS (52964-1001-1) |
| Product NDC | 52964-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SUS SCROFA PLACENTA |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120802 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | TMN K.K. |
| Substance Name | SUS SCROFA PLACENTA |
| Strength Number | 16000 |
| Strength Unit | mg/30mL |
| Pharmaceutical Classes |
