AMPICILLIN
- Product NDC
- 67850-023
- 11-digit product format
- 678500023
- Labeler code
- 67850
- Product ID
- 67850-023_8d1c1c38-c673-4a99-9a6b-f546c0379c5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ampicillin Injection
- Dosage form
- POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Methapharm Inc.
- Application
- ANDA090354
- Marketing category
- ANDA
- Marketing start
- 2019-03-06
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM
- Active strength
- 250 mg/250mg
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67850-023 | AMPICILLIN (AMPICILLIN INJECTION) POWDER, FOR SOLUTION [METHAPHARM INC.] | 9 | Legacy NDC | 20241207_3f6275f9-ee6f-4087-b672-5611d6870558.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67850-023-10 | 67850002310 | 10 VIAL in 1 PACKAGE (67850-023-10) > 250 mg in 1 VIAL (67850-023-00) | 10 vial | 2019-03-06 | 0000-00-00 | No | No | Current |