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meloxicam
meloxicam - 65841-050-16 - (meloxicam)
Drug Information of meloxicam
| Product NDC: | 65841-050 |
| Proprietary Name: | meloxicam |
| Non Proprietary Name: | meloxicam |
| Active Ingredient(s): | 7.5 mg/1 & nbsp; meloxicam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of meloxicam
| Product NDC: | 65841-050 |
| Labeler Name: | Cadila Healthcare Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077921 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060719 |
Package Information of meloxicam
| Package NDC: | 65841-050-16 |
| Package Description: | 90 TABLET in 1 BOTTLE (65841-050-16) |
NDC Information of meloxicam
| NDC Code | 65841-050-16 |
| Proprietary Name | meloxicam |
| Package Description | 90 TABLET in 1 BOTTLE (65841-050-16) |
| Product NDC | 65841-050 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | meloxicam |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060719 |
| Marketing Category Name | ANDA |
| Labeler Name | Cadila Healthcare Limited |
| Substance Name | MELOXICAM |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
