AMOXICILLIN
- Product NDC
- 61919-672
- 11-digit product format
- 619190672
- Labeler code
- 61919
- Product ID
- 61919-672_85916ec0-0a9f-fad0-e053-2a91aa0aeca4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMOXICILLIN
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- DIRECTRX
- Application
- ANDA065378
- Marketing category
- ANDA
- Marketing start
- 2019-04-02
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 200 mg/5mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-672-32 | 61919067232 | 100 mL in 1 BOTTLE (61919-672-32) | 100 ml | 2019-04-02 | 0000-00-00 | No | No | Current |