Product NDC: | 52389-117 |
Proprietary Name: | Pep-Back |
Non Proprietary Name: | Caffeine |
Active Ingredient(s): | 200 mg/1 & nbsp; Caffeine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52389-117 |
Labeler Name: | Alva-Amco Pharmacal Companies, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part340 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20070328 |
Package NDC: | 52389-117-28 |
Package Description: | 2 BLISTER PACK in 1 CARTON (52389-117-28) > 14 TABLET, FILM COATED in 1 BLISTER PACK (52389-117-01) |
NDC Code | 52389-117-28 |
Proprietary Name | Pep-Back |
Package Description | 2 BLISTER PACK in 1 CARTON (52389-117-28) > 14 TABLET, FILM COATED in 1 BLISTER PACK (52389-117-01) |
Product NDC | 52389-117 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Caffeine |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20070328 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Alva-Amco Pharmacal Companies, Inc. |
Substance Name | CAFFEINE |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes |