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Tetracycline Hydrochloride
Tetracycline Hydrochloride - 0591-2235-10 - (Tetracycline Hydrochloride)
Drug Information of Tetracycline Hydrochloride
| Product NDC: | 0591-2235 |
| Proprietary Name: | Tetracycline Hydrochloride |
| Non Proprietary Name: | Tetracycline Hydrochloride |
| Active Ingredient(s): | 500 mg/1 & nbsp; Tetracycline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tetracycline Hydrochloride
| Product NDC: | 0591-2235 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA061837 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101219 |
Package Information of Tetracycline Hydrochloride
| Package NDC: | 0591-2235-10 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE, PLASTIC (0591-2235-10) |
NDC Information of Tetracycline Hydrochloride
| NDC Code | 0591-2235-10 |
| Proprietary Name | Tetracycline Hydrochloride |
| Package Description | 1000 CAPSULE in 1 BOTTLE, PLASTIC (0591-2235-10) |
| Product NDC | 0591-2235 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tetracycline Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20101219 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | TETRACYCLINE HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Antimicrobial [EPC],Tetracyclines [Chemical/Ingredient] |
