Ampicillin
- Product NDC
- 68788-7139
- 11-digit product format
- 687887139
- Labeler code
- 68788
- Product ID
- 68788-7139_17dc6f9c-1a52-4ea4-bf9e-54a358044061
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA064082
- Marketing category
- ANDA
- Marketing start
- 2018-04-19
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN TRIHYDRATE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record