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Indomethacin
Indomethacin - 24236-621-24 - (indomethacin)
Drug Information of Indomethacin
| Product NDC: | 24236-621 |
| Proprietary Name: | Indomethacin |
| Non Proprietary Name: | indomethacin |
| Active Ingredient(s): | 50 mg/1 & nbsp; indomethacin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Indomethacin
| Product NDC: | 24236-621 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070624 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130318 |
Package Information of Indomethacin
| Package NDC: | 24236-621-24 |
| Package Description: | 200 CAPSULE in 1 CANISTER (24236-621-24) |
NDC Information of Indomethacin
| NDC Code | 24236-621-24 |
| Proprietary Name | Indomethacin |
| Package Description | 200 CAPSULE in 1 CANISTER (24236-621-24) |
| Product NDC | 24236-621 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | indomethacin |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130318 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | INDOMETHACIN |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
