← FDA Drug Approvals (Drugs@FDA)
AMMONIUM LACTATE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARMA CANADA · Approved 2004-05-28
Drug application
- FDA Application #
ANDA076216
- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- AMMONIUM LACTATE
- Generic name
- AMMONIUM LACTATE
- Active ingredients
- AMMONIUM LACTATE
- Dosage form
- LOTION
- Route
- TOPICAL
- Marketing status
- Prescription
- Sponsor
- SUN PHARMA CANADA
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- First approval
- 2004-05-28
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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