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ASPIRIN
ASPIRIN - 65437-038-07 - (ASPIRIN)
Drug Information of ASPIRIN
| Product NDC: | 65437-038 |
| Proprietary Name: | ASPIRIN |
| Non Proprietary Name: | ASPIRIN |
| Active Ingredient(s): | 325 mg/1 & nbsp; ASPIRIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ASPIRIN
| Product NDC: | 65437-038 |
| Labeler Name: | HIMPRIT PHARMACHEM PVT LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100301 |
Package Information of ASPIRIN
| Package NDC: | 65437-038-07 |
| Package Description: | 1 BAG in 1 DRUM (65437-038-07) > 75000 TABLET, FILM COATED in 1 BAG |
NDC Information of ASPIRIN
| NDC Code | 65437-038-07 |
| Proprietary Name | ASPIRIN |
| Package Description | 1 BAG in 1 DRUM (65437-038-07) > 75000 TABLET, FILM COATED in 1 BAG |
| Product NDC | 65437-038 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ASPIRIN |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | HIMPRIT PHARMACHEM PVT LTD |
| Substance Name | ASPIRIN |
| Strength Number | 325 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
