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Glycerin
Glycerin - 0713-0101-51 - (Glycerin)
Drug Information of Glycerin
| Product NDC: | 0713-0101 |
| Proprietary Name: | Glycerin |
| Non Proprietary Name: | Glycerin |
| Active Ingredient(s): | 2.1 g/1 & nbsp; Glycerin |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glycerin
| Product NDC: | 0713-0101 |
| Labeler Name: | G&W Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19870608 |
Package Information of Glycerin
| Package NDC: | 0713-0101-51 |
| Package Description: | 51 SUPPOSITORY in 1 JAR (0713-0101-51) |
NDC Information of Glycerin
| NDC Code | 0713-0101-51 |
| Proprietary Name | Glycerin |
| Package Description | 51 SUPPOSITORY in 1 JAR (0713-0101-51) |
| Product NDC | 0713-0101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Glycerin |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 19870608 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | G&W Laboratories, Inc. |
| Substance Name | GLYCERIN |
| Strength Number | 2.1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes |
