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demeclocycline hydrochloride
demeclocycline hydrochloride - 61748-115-01 - (demeclocycline hydrochloride)
Drug Information of demeclocycline hydrochloride
| Product NDC: | 61748-115 |
| Proprietary Name: | demeclocycline hydrochloride |
| Non Proprietary Name: | demeclocycline hydrochloride |
| Active Ingredient(s): | 150 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: | 61748-115 |
| Labeler Name: | VersaPharm Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065389 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081215 |
Package Information of demeclocycline hydrochloride
| Package NDC: | 61748-115-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (61748-115-01) |
NDC Information of demeclocycline hydrochloride
| NDC Code | 61748-115-01 |
| Proprietary Name | demeclocycline hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (61748-115-01) |
| Product NDC | 61748-115 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | demeclocycline hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20081215 |
| Marketing Category Name | ANDA |
| Labeler Name | VersaPharm Incorporated |
| Substance Name | DEMECLOCYCLINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Antimicrobial [EPC],Tetracyclines [Chemical/Ingredient] |
