SUMYCIN
- Product NDC
- 49884-733
- 11-digit product format
- 498840733
- Labeler code
- 49884
- Product ID
- 49884-733_1e4f1def-9e2e-4879-ace2-b20a8b3c2ff0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tetracycline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA061147
- Marketing category
- ANDA
- Marketing start
- 2017-04-04
- Marketing end
- 0000-00-00
- Substance
- TETRACYCLINE HYDROCHLORIDE
- Active strength
- 500 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49884-733-01 | 49884073301 | 100 TABLET, FILM COATED in 1 BOTTLE (49884-733-01) | 2017-04-04 | 0000-00-00 | No | No | Current |
| 49884-733-05 | 49884073305 | 500 TABLET, FILM COATED in 1 BOTTLE (49884-733-05) | 2017-04-04 | 0000-00-00 | No | No | Current |