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Subtilis
Subtilis - 49693-2301-1 - (Bacillus subtilis)
Drug Information of Subtilis
| Product NDC: | 49693-2301 |
| Proprietary Name: | Subtilis |
| Non Proprietary Name: | Bacillus subtilis |
| Active Ingredient(s): | 6 [hp_X]/5mL & nbsp; Bacillus subtilis |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Subtilis
| Product NDC: | 49693-2301 |
| Labeler Name: | USPharmaCo |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20091215 |
Package Information of Subtilis
| Package NDC: | 49693-2301-1 |
| Package Description: | 1 BOTTLE in 1 BOX (49693-2301-1) > 5 mL in 1 BOTTLE |
NDC Information of Subtilis
| NDC Code | 49693-2301-1 |
| Proprietary Name | Subtilis |
| Package Description | 1 BOTTLE in 1 BOX (49693-2301-1) > 5 mL in 1 BOTTLE |
| Product NDC | 49693-2301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bacillus subtilis |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20091215 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | USPharmaCo |
| Substance Name | BACILLUS SUBTILIS |
| Strength Number | 6 |
| Strength Unit | [hp_X]/5mL |
| Pharmaceutical Classes |
