Demeclocycline Hydrochloride
- Product NDC
- 60429-649
- 11-digit product format
- 604290649
- Labeler code
- 60429
- Product ID
- 60429-649_d44fab3a-5ef1-f637-e053-2a95a90a520f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Demeclocycline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA065447
- Marketing category
- ANDA
- Marketing start
- 2015-08-18
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-649-48 | 60429064948 | 48 TABLET, FILM COATED in 1 BOTTLE (60429-649-48) | 2016-02-05 | 0000-00-00 | No | No | Current |