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Demeclocycline Hydrochloride
Demeclocycline Hydrochloride - 0115-2122-02 - (Demeclocycline Hydrochloride)
Drug Information of Demeclocycline Hydrochloride
| Product NDC: | 0115-2122 |
| Proprietary Name: | Demeclocycline Hydrochloride |
| Non Proprietary Name: | Demeclocycline Hydrochloride |
| Active Ingredient(s): | 300 mg/1 & nbsp; Demeclocycline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Demeclocycline Hydrochloride
| Product NDC: | 0115-2122 |
| Labeler Name: | Global Pharmaceuticals, Division of Impax Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065094 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040322 |
Package Information of Demeclocycline Hydrochloride
| Package NDC: | 0115-2122-02 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (0115-2122-02) |
NDC Information of Demeclocycline Hydrochloride
| NDC Code | 0115-2122-02 |
| Proprietary Name | Demeclocycline Hydrochloride |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0115-2122-02) |
| Product NDC | 0115-2122 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Demeclocycline Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20040322 |
| Marketing Category Name | ANDA |
| Labeler Name | Global Pharmaceuticals, Division of Impax Laboratories, Inc. |
| Substance Name | DEMECLOCYCLINE HYDROCHLORIDE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Antimicrobial [EPC],Tetracyclines [Chemical/Ingredient] |
