demeclocycline hydrochloride
- Product NDC
- 61748-115
- 11-digit product format
- 617480115
- Labeler code
- 61748
- Product ID
- 61748-115_608c9c5a-a05c-4117-96ce-96ac0c2880dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- demeclocycline hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Versapharm Incorporated
- Application
- ANDA065389
- Marketing category
- ANDA
- Marketing start
- 2008-12-15
- 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
- 2021-12-31
- 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 |
|---|
| 61748-115-01 | 61748011501 | 100 TABLET, FILM COATED in 1 BOTTLE (61748-115-01) | 2008-12-15 | 0000-00-00 | No | No | Current |