Amoxicillin
- Product NDC
- 68071-4086
- 11-digit product format
- 680714086
- Labeler code
- 68071
- Product ID
- 68071-4086_bb2cb692-f5dc-ca49-e053-2a95a90aae96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065256
- Marketing category
- ANDA
- Marketing start
- 2005-11-09
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 875 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4086-2 | 68071408602 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-4086-2) | 2017-09-08 | 0000-00-00 | No | No | Current |