Demeclocycline Hydrochloride
- Product NDC
- 42291-265
- 11-digit product format
- 422910265
- Labeler code
- 42291
- Product ID
- 42291-265_8f764438-43fd-7cc2-e053-2995a90a9a1d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Demeclocycline
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA065425
- Marketing category
- ANDA
- Marketing start
- 2017-04-27
- Marketing end
- 0000-00-00
- Substance
- DEMECLOCYCLINE HYDROCHLORIDE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Tetracycline-class Antimicrobial [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record