Demeclocycline Hydrochloride
- Product NDC
- 42291-264
- 11-digit product format
- 422910264
- Labeler code
- 42291
- Product ID
- 42291-264_636137da-63e6-1e0b-e053-2991aa0a5d3e
- 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
- 150 mg/1
- Pharmacologic classes
- Tetracycline-class Antimicrobial [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record