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PROMETHEGAN
PROMETHEGAN - 0713-0132-10 - (Promethazine Hydrochloride)
Drug Information of PROMETHEGAN
| Product NDC: | 0713-0132 |
| Proprietary Name: | PROMETHEGAN |
| Non Proprietary Name: | Promethazine Hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; Promethazine Hydrochloride |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROMETHEGAN
| Product NDC: | 0713-0132 |
| Labeler Name: | G & W LABORATORIES, INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087165 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19870831 |
Package Information of PROMETHEGAN
| Package NDC: | 0713-0132-10 |
| Package Description: | 1000 SUPPOSITORY in 1 BOX (0713-0132-10) |
NDC Information of PROMETHEGAN
| NDC Code | 0713-0132-10 |
| Proprietary Name | PROMETHEGAN |
| Package Description | 1000 SUPPOSITORY in 1 BOX (0713-0132-10) |
| Product NDC | 0713-0132 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Promethazine Hydrochloride |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 19870831 |
| Marketing Category Name | ANDA |
| Labeler Name | G & W LABORATORIES, INC. |
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
