Home
>
National Drug Code (NDC)
>
Rx Act all day pain relief
Rx Act all day pain relief - 37808-490-62 - (Naproxen Sodium)
Drug Information of Rx Act all day pain relief
| Product NDC: | 37808-490 |
| Proprietary Name: | Rx Act all day pain relief |
| Non Proprietary Name: | Naproxen Sodium |
| Active Ingredient(s): | 220 mg/1 & nbsp; Naproxen Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rx Act all day pain relief
| Product NDC: | 37808-490 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074661 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970224 |
Package Information of Rx Act all day pain relief
| Package NDC: | 37808-490-62 |
| Package Description: | 1 BOTTLE in 1 CARTON (37808-490-62) > 24 TABLET in 1 BOTTLE |
NDC Information of Rx Act all day pain relief
| NDC Code | 37808-490-62 |
| Proprietary Name | Rx Act all day pain relief |
| Package Description | 1 BOTTLE in 1 CARTON (37808-490-62) > 24 TABLET in 1 BOTTLE |
| Product NDC | 37808-490 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naproxen Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19970224 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
