SUMYCIN
- Product NDC
- 49884-732
- 11-digit product format
- 498840732
- Labeler code
- 49884
- Product ID
- 49884-732_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
- 250 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 |
|---|
| 49884-732-01 | 49884073201 | 100 TABLET, FILM COATED in 1 BOTTLE (49884-732-01) | 2017-04-04 | 0000-00-00 | No | No | Current |
| 49884-732-10 | 49884073210 | 1000 TABLET, FILM COATED in 1 BOTTLE (49884-732-10) | 2017-04-04 | 0000-00-00 | No | No | Current |