Demeclocycline Hydrochloride
- Product NDC
- 62584-159
- 11-digit product format
- 625840159
- Labeler code
- 62584
- Product ID
- 62584-159_e8a2c3c1-bb4e-a7fa-e053-2995a90a52f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Demeclocycline Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA065425
- Marketing category
- ANDA
- Marketing start
- 2010-11-24
- Marketing end
- 2023-07-31
- Substance
- DEMECLOCYCLINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Tetracycline-class Antimicrobial [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62584-159-01 | 62584015901 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (62584-159-01) > 1 TABLET in 1 BLISTER PACK (62584-159-11) | 100 blister pack | 2010-11-24 | 0000-00-00 | No | No | Current |