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ACEPHEN
ACEPHEN - 0713-0165-10 - (Acetaminophen)
Drug Information of ACEPHEN
| Product NDC: | 0713-0165 |
| Proprietary Name: | ACEPHEN |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 650 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACEPHEN
| Product NDC: | 0713-0165 |
| Labeler Name: | G&W Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA072237 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19920327 |
Package Information of ACEPHEN
| Package NDC: | 0713-0165-10 |
| Package Description: | 1000 SUPPOSITORY in 1 BOX (0713-0165-10) |
NDC Information of ACEPHEN
| NDC Code | 0713-0165-10 |
| Proprietary Name | ACEPHEN |
| Package Description | 1000 SUPPOSITORY in 1 BOX (0713-0165-10) |
| Product NDC | 0713-0165 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 19920327 |
| Marketing Category Name | ANDA |
| Labeler Name | G&W Laboratories, Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
