Ampicillin
- Product NDC
- 67253-182
- 11-digit product format
- 672530182
- Labeler code
- 67253
- Product ID
- 67253-182_781ed9b9-e0ee-499b-8dc2-be2781091f42
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Par Pharmaceutical
- Application
- ANDA062982
- Marketing category
- ANDA
- Marketing start
- 1989-02-10
- Marketing end
- 2020-08-31
- Substance
- AMPICILLIN TRIHYDRATE
- Active strength
- 25 mg/mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record