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all day pain relief
all day pain relief - 37808-339-82 - (Naproxen sodium)
Drug Information of all day pain relief
| Product NDC: | 37808-339 |
| Proprietary Name: | all day pain relief |
| Non Proprietary Name: | Naproxen sodium |
| Active Ingredient(s): | 200 mg/1 & nbsp; Naproxen sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of all day pain relief
| Product NDC: | 37808-339 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074661 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080212 |
Package Information of all day pain relief
| Package NDC: | 37808-339-82 |
| Package Description: | 200 TABLET, FILM COATED in 1 BOTTLE (37808-339-82) |
NDC Information of all day pain relief
| NDC Code | 37808-339-82 |
| Proprietary Name | all day pain relief |
| Package Description | 200 TABLET, FILM COATED in 1 BOTTLE (37808-339-82) |
| Product NDC | 37808-339 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naproxen sodium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20080212 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
