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FOLIC ACID
FOLIC ACID - 76282-210-10 - (FOLIC ACID)
Drug Information of FOLIC ACID
| Product NDC: | 76282-210 |
| Proprietary Name: | FOLIC ACID |
| Non Proprietary Name: | FOLIC ACID |
| Active Ingredient(s): | 1 mg/1 & nbsp; FOLIC ACID |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FOLIC ACID
| Product NDC: | 76282-210 |
| Labeler Name: | Exelan Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090035 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100406 |
Package Information of FOLIC ACID
| Package NDC: | 76282-210-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (76282-210-10) |
NDC Information of FOLIC ACID
| NDC Code | 76282-210-10 |
| Proprietary Name | FOLIC ACID |
| Package Description | 1000 TABLET in 1 BOTTLE (76282-210-10) |
| Product NDC | 76282-210 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FOLIC ACID |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100406 |
| Marketing Category Name | ANDA |
| Labeler Name | Exelan Pharmaceuticals, Inc. |
| Substance Name | FOLIC ACID |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
